Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1131012
rs1131012
10 0.763 0.280 17 64350416 missense variant T/C snv 0.38 0.010 1.000 1 2013 2013
dbSNP: rs668
rs668
4 0.851 0.240 17 64377836 missense variant C/G;T snv 0.010 1.000 1 2013 2013