rs758712508, APC

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.
Hereditary Nonpolyposis Colorectal Cancer
1331 0.925 0.160 5 112838286 missense variant C/T snv 4.0E-06 0.010 1.000 1 2008 2008
Lynch Syndrome
CUI: C4552100
Disease: Lynch Syndrome
65 0.925 0.160 5 112838286 missense variant C/T snv 4.0E-06 0.010 1.000 1 2008 2008