rs63750070, MSH2

N. diseases: 3
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Colorectal cancer, hereditary nonpolyposis, type 1
179 0.882 0.160 2 47410245 missense variant T/C;G snv 0.800 1.000 37 1994 2017
Hereditary Nonpolyposis Colorectal Cancer
1331 0.882 0.160 2 47410245 missense variant T/C;G snv 0.700 1.000 8 2005 2011
Malignant neoplasm of gastrointestinal tract
55 0.882 0.160 2 47410245 missense variant T/C;G snv 0.010 1.000 1 2006 2006