Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750086
rs63750086
C 0.700 CausalMutation CLINVAR

dbSNP: rs63750875
rs63750875
0.020 GeneticVariation BEFREE Lifetime risks of CRC and EC in MSH2 A636P carriers are high even after adjusting for ascertainment. 21419771

2011

dbSNP: rs63750875
rs63750875
0.020 GeneticVariation BEFREE Genetic counseling and testing for the MSH2 A636P mutation is indicated for Ashkenazi Jewish women with an endometrial cancer, especially if the cancer is detected before the age of 70 years in women with a personal or family history of colorectal cancer. 18674656

2008

dbSNP: rs549467183
rs549467183
0.010 GeneticVariation BEFREE No disease-causing mutation within the coding sequences of the hMLH1/hMSH2 and PTEN genes was found in patients with EC who had the mutator phenotype (MSI positive and IHC negative), except for a newly described hMLH1 missense mutation, Ile655Val, that was observed in 1 of 27 patients (4%). 12115348

2002

dbSNP: rs864622121
rs864622121
0.010 GeneticVariation BEFREE No disease-causing mutation within the coding sequences of the hMLH1/hMSH2 and PTEN genes was found in patients with EC who had the mutator phenotype (MSI positive and IHC negative), except for a newly described hMLH1 missense mutation, Ile655Val, that was observed in 1 of 27 patients (4%). 12115348

2002