rs17224367, 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 47429833 missense variant C/G;T snv 1.5E-03 0.700 0
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.882 0.160 2 47429833 missense variant C/G;T snv 1.5E-03 0.700 0
Malignant neoplasm of gastrointestinal tract
55 0.882 0.160 2 47429833 missense variant C/G;T snv 1.5E-03 0.010 1.000 1 2006 2006