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What is the type of genetic variation for RS1566233014 SNP? | The variation is a Duplication. |
Which condition is asociated with RS587778833 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/RsRS587778833 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778833 SNP. |
In which chromosome is RS587778833 SNP located? | It is located in the chromosome 13. |
Which methods support the evidence found for the RS587778833 SNP? | Associated methods are: research. |
What is the clinical significance of RS587778833 SNP, is it benign or pathogenic? | It is Pathogenic. |
How long is the variation length for RS587778833 SNP? | The variation length is 1 base pairs. |
What is the origin for RS587778833 SNP? | The origin is somatic. |
What is the type of genetic variation for RS587778833 SNP? | The variation is a single nucleotide variant. |
What is the genetic molecular consequence for RS587778833 SNP? | The resulting gene consequence is a nonsense. |
Which condition is asociated with RS587778865 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/RsRS587778865 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778865 SNP. |
In which chromosome is RS587778865 SNP located? | It is located in the chromosome 13. |
Which methods support the evidence found for the RS587778865 SNP? | Associated methods are: research. |
What is the clinical significance of RS587778865 SNP, is it benign or pathogenic? | It is Pathogenic. |
How long is the variation length for RS587778865 SNP? | The variation length is 1 base pairs. |
What is the origin for RS587778865 SNP? | The origin is somatic. |
What is the type of genetic variation for RS587778865 SNP? | The variation is a single nucleotide variant. |
What is the genetic molecular consequence for RS587778865 SNP? | The resulting gene consequence is a nonsense. |
Which condition is asociated with RS587778866 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/RsRS587778866 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778866 SNP. |
In which chromosome is RS587778866 SNP located? | It is located in the chromosome 13. |
Which methods support the evidence found for the RS587778866 SNP? | Associated methods are: research. |
What is the clinical significance of RS587778866 SNP, is it benign or pathogenic? | It is Pathogenic. |
How long is the variation length for RS587778866 SNP? | The variation length is 1 base pairs. |
What is the origin for RS587778866 SNP? | The origin is somatic. |
What is the type of genetic variation for RS587778866 SNP? | The variation is a single nucleotide variant. |
What is the genetic molecular consequence for RS587778866 SNP? | The resulting gene consequence is a missense variant. |
Which condition is asociated with RS587778834 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/RsRS587778834 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778834 SNP. |
In which chromosome is RS587778834 SNP located? | It is located in the chromosome 13. |
Which methods support the evidence found for the RS587778834 SNP? | Associated methods are: research, clinical testing. |
What is the clinical significance of RS587778834 SNP, is it benign or pathogenic? | It is Uncertain significance. |
How long is the variation length for RS587778834 SNP? | The variation length is 1 base pairs. |
What is the origin for RS587778834 SNP? | The origin is somatic. |
What is the type of genetic variation for RS587778834 SNP? | The variation is a single nucleotide variant. |
What is the genetic molecular consequence for RS587778834 SNP? | The resulting gene consequence is a missense variant. |
Which condition is asociated with RS587778859 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/RsRS587778859 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778859 SNP. |
In which chromosome is RS587778859 SNP located? | It is located in the chromosome 13. |
Which methods support the evidence found for the RS587778859 SNP? | Associated methods are: clinical testing. |
What is the clinical significance of RS587778859 SNP, is it benign or pathogenic? | It is Pathogenic. |
How long is the variation length for RS587778859 SNP? | The variation length is 1 base pairs. |
What is the origin for RS587778859 SNP? | The origin is somatic. |
What is the type of genetic variation for RS587778859 SNP? | The variation is a single nucleotide variant. |
What is the genetic molecular consequence for RS587778859 SNP? | The resulting gene consequence is a missense variant. |
Which condition is asociated with RS587778835 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/RsRS587778835 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778835 SNP. |
In which chromosome is RS587778835 SNP located? | It is located in the chromosome 13. |
Which methods support the evidence found for the RS587778835 SNP? | Associated methods are: clinical testing. |
What is the clinical significance of RS587778835 SNP, is it benign or pathogenic? | It is Pathogenic. |
How long is the variation length for RS587778835 SNP? | The variation length is 1 base pairs. |
What is the origin for RS587778835 SNP? | The origin is somatic. |
What is the type of genetic variation for RS587778835 SNP? | The variation is a single nucleotide variant. |
What is the genetic molecular consequence for RS587778835 SNP? | The resulting gene consequence is a missense variant. |
Which condition is asociated with RS587778868 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/RsRS587778868 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778868 SNP. |
In which chromosome is RS587778868 SNP located? | It is located in the chromosome 13. |
Which methods support the evidence found for the RS587778868 SNP? | Associated methods are: clinical testing. |
What is the clinical significance of RS587778868 SNP, is it benign or pathogenic? | It is Pathogenic. |
How long is the variation length for RS587778868 SNP? | The variation length is 1 base pairs. |
What is the origin for RS587778868 SNP? | The origin is somatic. |
What is the type of genetic variation for RS587778868 SNP? | The variation is a single nucleotide variant. |
What is the genetic molecular consequence for RS587778868 SNP? | The resulting gene consequence is a nonsense. |
Which condition is asociated with RS587778861 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/RsRS587778861 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778861 SNP. |
In which chromosome is RS587778861 SNP located? | It is located in the chromosome 13. |
Which methods support the evidence found for the RS587778861 SNP? | Associated methods are: clinical testing. |
What is the clinical significance of RS587778861 SNP, is it benign or pathogenic? | It is Pathogenic. |
How long is the variation length for RS587778861 SNP? | The variation length is 1 base pairs. |
What is the origin for RS587778861 SNP? | The origin is somatic. |
What is the type of genetic variation for RS587778861 SNP? | The variation is a single nucleotide variant. |
What is the genetic molecular consequence for RS587778861 SNP? | The resulting gene consequence is a nonsense. |
Which condition is asociated with RS587778826 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/RsRS587778826 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778826 SNP. |
In which chromosome is RS587778826 SNP located? | It is located in the chromosome 13. |
Which methods support the evidence found for the RS587778826 SNP? | Associated methods are: clinical testing. |
What is the clinical significance of RS587778826 SNP, is it benign or pathogenic? | It is Pathogenic. |
How long is the variation length for RS587778826 SNP? | The variation length is 1 base pairs. |
What is the origin for RS587778826 SNP? | The origin is somatic. |
What is the type of genetic variation for RS587778826 SNP? | The variation is a single nucleotide variant. |
What is the genetic molecular consequence for RS587778826 SNP? | The resulting gene consequence is a nonsense. |
Which condition is asociated with 132325? | 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/Rs132325. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/132325. |
In which chromosome is 132325 located? | It is located in the chromosome 13. |
Which methods support the evidence found for the 132325? | Associated methods are: research. |
What is the clinical significance of 132325, is it benign or pathogenic? | It is Pathogenic. |
How long is the variation length for 132325? | The variation length is None base pairs. |
What is the origin for 132325? | The origin is somatic. |
What is the type of genetic variation for 132325? | The variation is a Variation. |
Which condition is asociated with RS587778843 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/RsRS587778843 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778843 SNP. |
In which chromosome is RS587778843 SNP located? | It is located in the chromosome 13. |
Which methods support the evidence found for the RS587778843 SNP? | Associated methods are: clinical testing. |
What is the clinical significance of RS587778843 SNP, is it benign or pathogenic? | It is Pathogenic. |
How long is the variation length for RS587778843 SNP? | The variation length is 1 base pairs. |
What is the origin for RS587778843 SNP? | The origin is somatic. |
What is the type of genetic variation for RS587778843 SNP? | The variation is a single nucleotide variant. |
What is the genetic molecular consequence for RS587778843 SNP? | The resulting gene consequence is a nonsense. |
Which condition is asociated with RS587778855 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/RsRS587778855 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778855 SNP. |
In which chromosome is RS587778855 SNP located? | It is located in the chromosome 13. |
Which methods support the evidence found for the RS587778855 SNP? | Associated methods are: research. |
What is the clinical significance of RS587778855 SNP, is it benign or pathogenic? | It is Pathogenic. |
How long is the variation length for RS587778855 SNP? | The variation length is 1 base pairs. |
What is the origin for RS587778855 SNP? | The origin is germline. |
What is the type of genetic variation for RS587778855 SNP? | The variation is a single nucleotide variant. |
What is the genetic molecular consequence for RS587778855 SNP? | The resulting gene consequence is a nonsense. |
Which condition is asociated with RS587778856 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/RsRS587778856 SNP. The NCBI page is https://www.ncbi.nlm.nih.gov/snp/RS587778856 SNP. |
In which chromosome is RS587778856 SNP located? | It is located in the chromosome 13. |
Which methods support the evidence found for the RS587778856 SNP? | Associated methods are: clinical testing. |
What is the clinical significance of RS587778856 SNP, is it benign or pathogenic? | It is Uncertain significance. |