rs3803185, ARL11

N. diseases: 19
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.
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.708 0.320 13 49630889 missense variant T/C;G snv 0.39 0.010 1.000 1 2006 2006