Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63750574
rs63750574
MSH2
T 0.700 CausalMutation CLINVAR Mismatch repair gene mutation analysis and colonoscopy surveillance in Chinese Lynch syndrome families. 23640085

2013
dbSNP: rs63750574
rs63750574
MSH2
T 0.700 CausalMutation CLINVAR Clinical features and mismatch repair gene mutation screening in Chinese patients with hereditary nonpolyposis colorectal carcinoma. 15309712

2004