Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 36
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 31
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs1801270 0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05 22
rs1194611372 0.763 0.320 1 152032679 missense variant A/C snv 9