Gene: MSH2 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750875
rs63750875
MSH2
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
MSH2
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