Variant: rs1060501991 

    present in Gene: MSH2
    present in Chromosome: 2
    Position on Chromosome: 47480695
    Alleles of this Variant: G/A;C

rs1060501991 in MSH2 gene and Hereditary Nonpolyposis Colorectal Neoplasms PMID 24362816 2014 Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.

PMID 15849733 2005 Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer.