Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs1475170339 0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs367543041 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs63751287 0.742 0.120 14 73192792 missense variant A/G;T snv 13
rs80356726 0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 12