rs63751110, MSH2

N. diseases: 2
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.
Glioma
CUI: C0017638
Disease: Glioma
353 0.925 0.160 2 47410322 missense variant T/C;G snv 0.700 0
Hereditary Nonpolyposis Colorectal Cancer
1331 0.925 0.160 2 47410322 missense variant T/C;G snv 0.700 0