rs575031539, CDKN2A

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.
melanoma
CUI: C0025202
Disease: melanoma
515 0.925 0.080 9 21971020 missense variant C/G;T snv 4.2E-06 0.010 1.000 1 2007 2007
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.925 0.080 9 21971020 missense variant C/G;T snv 4.2E-06 0.010 1.000 1 2007 2007