Toyokolabs/retinoblastoma · Datasets at Hugging Face

instruction stringlengths 30 82	output stringlengths 13 790
Which methods support the evidence found for the RS1593529908 SNP?	Associated methods are: clinical testing.
What is the clinical significance of RS1593529908 SNP, is it benign or pathogenic?	It is Likely benign.
How long is the variation length for RS1593529908 SNP?	The variation length is 1 base pairs.
What is the origin for RS1593529908 SNP?	The origin is germline.
What is the type of genetic variation for RS1593529908 SNP?	The variation is a single nucleotide variant.
What is the genetic molecular consequence for RS1593529908 SNP?	The resulting gene consequence is a synonymous variant.
Which condition is asociated with RS763895695 SNP?	Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS763895695 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS763895695 SNP.
In which chromosome is RS763895695 SNP located?	It is located in the chromosome 13.
Which methods support the evidence found for the RS763895695 SNP?	Associated methods are: clinical testing.
What is the clinical significance of RS763895695 SNP, is it benign or pathogenic?	It is Likely benign.
How long is the variation length for RS763895695 SNP?	The variation length is 1 base pairs.
What is the origin for RS763895695 SNP?	The origin is germline.
What is the type of genetic variation for RS763895695 SNP?	The variation is a single nucleotide variant.
What is the genetic molecular consequence for RS763895695 SNP?	The resulting gene consequence is a intron variant.
Which condition is asociated with RS780654106 SNP?	Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS780654106 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS780654106 SNP.
In which chromosome is RS780654106 SNP located?	It is located in the chromosome 13.
Which methods support the evidence found for the RS780654106 SNP?	Associated methods are: clinical testing.
What is the clinical significance of RS780654106 SNP, is it benign or pathogenic?	It is Likely benign.
How long is the variation length for RS780654106 SNP?	The variation length is 1 base pairs.
What is the origin for RS780654106 SNP?	The origin is germline.
What is the type of genetic variation for RS780654106 SNP?	The variation is a single nucleotide variant.
What is the genetic molecular consequence for RS780654106 SNP?	The resulting gene consequence is a synonymous variant.
Which condition is asociated with RS1014225642 SNP?	Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1014225642 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1014225642 SNP.
In which chromosome is RS1014225642 SNP located?	It is located in the chromosome 13.
Which methods support the evidence found for the RS1014225642 SNP?	Associated methods are: clinical testing.
What is the clinical significance of RS1014225642 SNP, is it benign or pathogenic?	It is Likely benign.
How long is the variation length for RS1014225642 SNP?	The variation length is 1 base pairs.
What is the origin for RS1014225642 SNP?	The origin is germline.
What is the type of genetic variation for RS1014225642 SNP?	The variation is a single nucleotide variant.
What is the genetic molecular consequence for RS1014225642 SNP?	The resulting gene consequence is a synonymous variant.
Which condition is asociated with RS1593414358 SNP?	Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593414358 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593414358 SNP.
In which chromosome is RS1593414358 SNP located?	It is located in the chromosome 13.
Which methods support the evidence found for the RS1593414358 SNP?	Associated methods are: clinical testing.
What is the clinical significance of RS1593414358 SNP, is it benign or pathogenic?	It is Likely benign.
How long is the variation length for RS1593414358 SNP?	The variation length is 1 base pairs.
What is the origin for RS1593414358 SNP?	The origin is germline.
What is the type of genetic variation for RS1593414358 SNP?	The variation is a single nucleotide variant.
What is the genetic molecular consequence for RS1593414358 SNP?	The resulting gene consequence is a synonymous variant.
Which condition is asociated with RS771620677 SNP?	Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS771620677 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS771620677 SNP.
In which chromosome is RS771620677 SNP located?	It is located in the chromosome 13.
Which methods support the evidence found for the RS771620677 SNP?	Associated methods are: clinical testing.
What is the clinical significance of RS771620677 SNP, is it benign or pathogenic?	It is Likely benign.
How long is the variation length for RS771620677 SNP?	The variation length is 1 base pairs.
What is the origin for RS771620677 SNP?	The origin is germline.
What is the type of genetic variation for RS771620677 SNP?	The variation is a single nucleotide variant.
What is the genetic molecular consequence for RS771620677 SNP?	The resulting gene consequence is a synonymous variant.
Which condition is asociated with RS1593437266 SNP?	Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593437266 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593437266 SNP.
In which chromosome is RS1593437266 SNP located?	It is located in the chromosome 13.
Which methods support the evidence found for the RS1593437266 SNP?	Associated methods are: clinical testing.
What is the clinical significance of RS1593437266 SNP, is it benign or pathogenic?	It is Likely benign.
How long is the variation length for RS1593437266 SNP?	The variation length is 1 base pairs.
What is the origin for RS1593437266 SNP?	The origin is germline.
What is the type of genetic variation for RS1593437266 SNP?	The variation is a single nucleotide variant.
What is the genetic molecular consequence for RS1593437266 SNP?	The resulting gene consequence is a intron variant.
Which condition is asociated with RS1379479714 SNP?	Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1379479714 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1379479714 SNP.
In which chromosome is RS1379479714 SNP located?	It is located in the chromosome 13.
Which methods support the evidence found for the RS1379479714 SNP?	Associated methods are: clinical testing.
What is the clinical significance of RS1379479714 SNP, is it benign or pathogenic?	It is Likely benign.
How long is the variation length for RS1379479714 SNP?	The variation length is 1 base pairs.
What is the origin for RS1379479714 SNP?	The origin is germline.
What is the type of genetic variation for RS1379479714 SNP?	The variation is a single nucleotide variant.
What is the genetic molecular consequence for RS1379479714 SNP?	The resulting gene consequence is a synonymous variant.
Which condition is asociated with RS775381228 SNP?	Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS775381228 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS775381228 SNP.
In which chromosome is RS775381228 SNP located?	It is located in the chromosome 13.
Which methods support the evidence found for the RS775381228 SNP?	Associated methods are: clinical testing.
What is the clinical significance of RS775381228 SNP, is it benign or pathogenic?	It is Likely benign.
How long is the variation length for RS775381228 SNP?	The variation length is 1 base pairs.
What is the origin for RS775381228 SNP?	The origin is germline.
What is the type of genetic variation for RS775381228 SNP?	The variation is a single nucleotide variant.
What is the genetic molecular consequence for RS775381228 SNP?	The resulting gene consequence is a synonymous variant.
Which condition is asociated with RS1593532040 SNP?	Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593532040 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593532040 SNP.
In which chromosome is RS1593532040 SNP located?	It is located in the chromosome 13.
Which methods support the evidence found for the RS1593532040 SNP?	Associated methods are: clinical testing.
What is the clinical significance of RS1593532040 SNP, is it benign or pathogenic?	It is Likely benign.
How long is the variation length for RS1593532040 SNP?	The variation length is 1 base pairs.
What is the origin for RS1593532040 SNP?	The origin is germline.
What is the type of genetic variation for RS1593532040 SNP?	The variation is a single nucleotide variant.
What is the genetic molecular consequence for RS1593532040 SNP?	The resulting gene consequence is a synonymous variant.
Which condition is asociated with RS879124999 SNP?	Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS879124999 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS879124999 SNP.
In which chromosome is RS879124999 SNP located?	It is located in the chromosome 13.
Which methods support the evidence found for the RS879124999 SNP?	Associated methods are: clinical testing.
What is the clinical significance of RS879124999 SNP, is it benign or pathogenic?	It is Likely benign.
How long is the variation length for RS879124999 SNP?	The variation length is 1 base pairs.
What is the origin for RS879124999 SNP?	The origin is germline.
What is the type of genetic variation for RS879124999 SNP?	The variation is a single nucleotide variant.
What is the genetic molecular consequence for RS879124999 SNP?	The resulting gene consequence is a synonymous variant.
Which condition is asociated with RS1593443613 SNP?	Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593443613 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593443613 SNP.
In which chromosome is RS1593443613 SNP located?	It is located in the chromosome 13.
Which methods support the evidence found for the RS1593443613 SNP?	Associated methods are: clinical testing.
What is the clinical significance of RS1593443613 SNP, is it benign or pathogenic?	It is Likely benign.
How long is the variation length for RS1593443613 SNP?	The variation length is 4 base pairs.
What is the origin for RS1593443613 SNP?	The origin is germline.
What is the type of genetic variation for RS1593443613 SNP?	The variation is a Deletion.
What is the genetic molecular consequence for RS1593443613 SNP?	The resulting gene consequence is a intron variant.
Which condition is asociated with RS1304775415 SNP?	Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1304775415 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1304775415 SNP.
In which chromosome is RS1304775415 SNP located?	It is located in the chromosome 13.
Which methods support the evidence found for the RS1304775415 SNP?	Associated methods are: clinical testing.
What is the clinical significance of RS1304775415 SNP, is it benign or pathogenic?	It is Likely benign.
How long is the variation length for RS1304775415 SNP?	The variation length is 1 base pairs.
What is the origin for RS1304775415 SNP?	The origin is germline.

Which methods support the evidence found for the RS1593529908 SNP?

Associated methods are: clinical testing.

What is the clinical significance of RS1593529908 SNP, is it benign or pathogenic?

It is Likely benign.

How long is the variation length for RS1593529908 SNP?

The variation length is 1 base pairs.

What is the origin for RS1593529908 SNP?

The origin is germline.

What is the type of genetic variation for RS1593529908 SNP?

The variation is a single nucleotide variant.

What is the genetic molecular consequence for RS1593529908 SNP?

The resulting gene consequence is a synonymous variant.

Which condition is asociated with RS763895695 SNP?

Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS763895695 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS763895695 SNP.

In which chromosome is RS763895695 SNP located?

It is located in the chromosome 13.

Which methods support the evidence found for the RS763895695 SNP?

Associated methods are: clinical testing.

What is the clinical significance of RS763895695 SNP, is it benign or pathogenic?

It is Likely benign.

How long is the variation length for RS763895695 SNP?

The variation length is 1 base pairs.

What is the origin for RS763895695 SNP?

The origin is germline.

What is the type of genetic variation for RS763895695 SNP?

The variation is a single nucleotide variant.

What is the genetic molecular consequence for RS763895695 SNP?

The resulting gene consequence is a intron variant.

Which condition is asociated with RS780654106 SNP?

Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS780654106 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS780654106 SNP.

In which chromosome is RS780654106 SNP located?

It is located in the chromosome 13.

Which methods support the evidence found for the RS780654106 SNP?

Associated methods are: clinical testing.

What is the clinical significance of RS780654106 SNP, is it benign or pathogenic?

It is Likely benign.

How long is the variation length for RS780654106 SNP?

The variation length is 1 base pairs.

What is the origin for RS780654106 SNP?

The origin is germline.

What is the type of genetic variation for RS780654106 SNP?

The variation is a single nucleotide variant.

What is the genetic molecular consequence for RS780654106 SNP?

The resulting gene consequence is a synonymous variant.

Which condition is asociated with RS1014225642 SNP?

Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1014225642 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1014225642 SNP.

In which chromosome is RS1014225642 SNP located?

It is located in the chromosome 13.

Which methods support the evidence found for the RS1014225642 SNP?

Associated methods are: clinical testing.

What is the clinical significance of RS1014225642 SNP, is it benign or pathogenic?

It is Likely benign.

How long is the variation length for RS1014225642 SNP?

The variation length is 1 base pairs.

What is the origin for RS1014225642 SNP?

The origin is germline.

What is the type of genetic variation for RS1014225642 SNP?

The variation is a single nucleotide variant.

What is the genetic molecular consequence for RS1014225642 SNP?

The resulting gene consequence is a synonymous variant.

Which condition is asociated with RS1593414358 SNP?

Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593414358 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593414358 SNP.

In which chromosome is RS1593414358 SNP located?

It is located in the chromosome 13.

Which methods support the evidence found for the RS1593414358 SNP?

Associated methods are: clinical testing.

What is the clinical significance of RS1593414358 SNP, is it benign or pathogenic?

It is Likely benign.

How long is the variation length for RS1593414358 SNP?

The variation length is 1 base pairs.

What is the origin for RS1593414358 SNP?

The origin is germline.

What is the type of genetic variation for RS1593414358 SNP?

The variation is a single nucleotide variant.

What is the genetic molecular consequence for RS1593414358 SNP?

The resulting gene consequence is a synonymous variant.

Which condition is asociated with RS771620677 SNP?

Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS771620677 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS771620677 SNP.

In which chromosome is RS771620677 SNP located?

It is located in the chromosome 13.

Which methods support the evidence found for the RS771620677 SNP?

Associated methods are: clinical testing.

What is the clinical significance of RS771620677 SNP, is it benign or pathogenic?

It is Likely benign.

How long is the variation length for RS771620677 SNP?

The variation length is 1 base pairs.

What is the origin for RS771620677 SNP?

The origin is germline.

What is the type of genetic variation for RS771620677 SNP?

The variation is a single nucleotide variant.

What is the genetic molecular consequence for RS771620677 SNP?

The resulting gene consequence is a synonymous variant.

Which condition is asociated with RS1593437266 SNP?

Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593437266 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593437266 SNP.

In which chromosome is RS1593437266 SNP located?

It is located in the chromosome 13.

Which methods support the evidence found for the RS1593437266 SNP?

Associated methods are: clinical testing.

What is the clinical significance of RS1593437266 SNP, is it benign or pathogenic?

It is Likely benign.

How long is the variation length for RS1593437266 SNP?

The variation length is 1 base pairs.

What is the origin for RS1593437266 SNP?

The origin is germline.

What is the type of genetic variation for RS1593437266 SNP?

The variation is a single nucleotide variant.

What is the genetic molecular consequence for RS1593437266 SNP?

The resulting gene consequence is a intron variant.

Which condition is asociated with RS1379479714 SNP?

Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1379479714 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1379479714 SNP.

In which chromosome is RS1379479714 SNP located?

It is located in the chromosome 13.

Which methods support the evidence found for the RS1379479714 SNP?

Associated methods are: clinical testing.

What is the clinical significance of RS1379479714 SNP, is it benign or pathogenic?

It is Likely benign.

How long is the variation length for RS1379479714 SNP?

The variation length is 1 base pairs.

What is the origin for RS1379479714 SNP?

The origin is germline.

What is the type of genetic variation for RS1379479714 SNP?

The variation is a single nucleotide variant.

What is the genetic molecular consequence for RS1379479714 SNP?

The resulting gene consequence is a synonymous variant.

Which condition is asociated with RS775381228 SNP?

Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS775381228 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS775381228 SNP.

In which chromosome is RS775381228 SNP located?

It is located in the chromosome 13.

Which methods support the evidence found for the RS775381228 SNP?

Associated methods are: clinical testing.

What is the clinical significance of RS775381228 SNP, is it benign or pathogenic?

It is Likely benign.

How long is the variation length for RS775381228 SNP?

The variation length is 1 base pairs.

What is the origin for RS775381228 SNP?

The origin is germline.

What is the type of genetic variation for RS775381228 SNP?

The variation is a single nucleotide variant.

What is the genetic molecular consequence for RS775381228 SNP?

The resulting gene consequence is a synonymous variant.

Which condition is asociated with RS1593532040 SNP?

Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593532040 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593532040 SNP.

In which chromosome is RS1593532040 SNP located?

It is located in the chromosome 13.

Which methods support the evidence found for the RS1593532040 SNP?

Associated methods are: clinical testing.

What is the clinical significance of RS1593532040 SNP, is it benign or pathogenic?

It is Likely benign.

How long is the variation length for RS1593532040 SNP?

The variation length is 1 base pairs.

What is the origin for RS1593532040 SNP?

The origin is germline.

What is the type of genetic variation for RS1593532040 SNP?

The variation is a single nucleotide variant.

What is the genetic molecular consequence for RS1593532040 SNP?

The resulting gene consequence is a synonymous variant.

Which condition is asociated with RS879124999 SNP?

Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS879124999 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS879124999 SNP.

In which chromosome is RS879124999 SNP located?

It is located in the chromosome 13.

Which methods support the evidence found for the RS879124999 SNP?

Associated methods are: clinical testing.

What is the clinical significance of RS879124999 SNP, is it benign or pathogenic?

It is Likely benign.

How long is the variation length for RS879124999 SNP?

The variation length is 1 base pairs.

What is the origin for RS879124999 SNP?

The origin is germline.

What is the type of genetic variation for RS879124999 SNP?

The variation is a single nucleotide variant.

What is the genetic molecular consequence for RS879124999 SNP?

The resulting gene consequence is a synonymous variant.

Which condition is asociated with RS1593443613 SNP?

Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1593443613 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1593443613 SNP.

In which chromosome is RS1593443613 SNP located?

It is located in the chromosome 13.

Which methods support the evidence found for the RS1593443613 SNP?

Associated methods are: clinical testing.

What is the clinical significance of RS1593443613 SNP, is it benign or pathogenic?

It is Likely benign.

How long is the variation length for RS1593443613 SNP?

The variation length is 4 base pairs.

What is the origin for RS1593443613 SNP?

The origin is germline.

What is the type of genetic variation for RS1593443613 SNP?

The variation is a Deletion.

What is the genetic molecular consequence for RS1593443613 SNP?

The resulting gene consequence is a intron variant.

Which condition is asociated with RS1304775415 SNP?

Retinoblastoma is a malignant tumor of the developing retina that occurs in children, usually before age five years. Retinoblastoma develops from cells that have cancer-predisposing variants in both copies of RB1. Retinoblastoma may be unifocal or multifocal. About 60% of affected individuals have unilateral retinoblastoma with a mean age of diagnosis of 24 months; about 40% have bilateral retinoblastoma with a mean age of diagnosis of 15 months. Heritable retinoblastoma is an autosomal dominant susceptibility for retinoblastoma. Individuals with heritable retinoblastoma are also at increased risk of developing non-ocular tumors. The associated SNPedia page is https://www.snpedia.com/index.php/RsRS1304775415 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS1304775415 SNP.

In which chromosome is RS1304775415 SNP located?

It is located in the chromosome 13.

Which methods support the evidence found for the RS1304775415 SNP?

Associated methods are: clinical testing.

What is the clinical significance of RS1304775415 SNP, is it benign or pathogenic?

It is Likely benign.

How long is the variation length for RS1304775415 SNP?

The variation length is 1 base pairs.

What is the origin for RS1304775415 SNP?

The origin is germline.