Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1064794096 1.000 0.040 10 87864514 missense variant A/C;T snv 1
rs121909233 1.000 0.040 10 87864524 missense variant G/A snv 1
rs786204929 0.752 0.200 10 87933144 stop gained G/A;T snv 1
rs587782603 1.000 0.040 10 87952118 stop gained G/A;T snv 1
rs1554893792 1.000 0.040 10 87894052 missense variant G/A snv 1
rs786202398 0.925 0.080 10 87925518 stop gained T/A;G snv 1
rs121909225 0.790 0.160 10 87894049 missense variant T/C;G snv 1
rs587782350 0.776 0.160 10 87957955 missense variant C/T snv 1
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 1
rs587782360 0.851 0.280 10 87933162 missense variant A/G snv 1
rs121909229 0.683 0.400 10 87933148 missense variant G/A;C;T snv 1
rs121909222 0.742 0.240 10 87933127 missense variant A/G snv 1
rs121909223 0.790 0.160 10 87933129 missense variant T/C;G snv 1
rs786204863 1.000 0.080 10 87952119 missense variant G/T snv 1
rs121909226 0.790 0.160 10 87925557 missense variant T/C snv 1
rs121909218 0.672 0.360 10 87933145 missense variant G/A snv 1
rs121909221 0.790 0.160 10 87952135 missense variant T/A snv 1
rs121909230 0.925 0.080 10 87933094 missense variant T/C snv 1
rs1554825652 1.000 0.080 10 87961113 missense variant T/G snv 1
rs398123317 0.790 0.160 10 87925550 missense variant T/A;C;G snv 1
rs1060500126 0.790 0.160 10 87933223 missense variant A/C;G snv 1
rs786204859 0.925 0.080 10 87933166 missense variant G/A snv 1
rs587782343 0.851 0.200 10 87933073 missense variant G/A snv 1
rs398123314 1.000 0.080 10 87961118 missense variant G/A;C snv 1
rs786204855 1.000 0.080 10 87894084 missense variant A/G snv 1