rs10235657

This variant is located in the POT1 gene.

GWAS Catalog Trait Associations (1)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

renal carcinoma

Allele G
OR 1.06
p 2.0e-8
N 864,690
Large GWAS
multi-ancestry

ClinVar annotation

Benign☆☆☆
1 submitter
View on ClinVar →

About POT1

This gene is a member of the telombin family and encodes a nuclear protein involved in telomere maintenance. Specifically, this protein functions as a member of a multi-protein complex that binds to the TTAGGG repeats of telomeres, regulating telomere length and protecting chromosome ends from illegitimate recombination, catastrophic chromosome instability, and abnormal chromosome segregation. Increased transcriptional expression of this gene is associated with stomach carcinogenesis and its progression. Alternatively spliced transcript variants have been described. [provided by RefSeq, Jul 2008]

View all POT1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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