Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519945 0.776 0.200 12 132673703 missense variant C/A;T snv 4
rs121913361 0.807 0.280 7 140753349 missense variant C/A;G;T snv 6
rs772110575 0.807 0.160 3 179198938 missense variant G/A;T snv 4.0E-06 6
rs1057519917 0.807 0.160 1 11124517 missense variant A/G;T snv 7
rs749415085 0.807 0.160 3 179198937 missense variant C/A;G;T snv 7
rs759610249 0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs1057519929 0.776 0.320 3 179199066 missense variant G/A snv 9
rs1057519941 0.776 0.240 3 179203761 missense variant T/C;G snv 9
rs587777894 0.776 0.240 1 11124516 missense variant G/A;T snv 9
rs1057519938 0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs1057519939 0.776 0.160 3 179203763 missense variant A/C snv 10
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 10
rs1057519884 0.752 0.240 16 3738616 missense variant C/A;T snv 11
rs1057519933 0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519934 0.790 0.240 3 179199158 missense variant G/C snv 11
rs1057519935 0.790 0.240 3 179199157 missense variant A/G snv 11
rs1057519936 0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs1057519937 0.776 0.200 3 179234285 missense variant T/C snv 11
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 11
rs587780071 0.732 0.240 17 7674951 missense variant G/A snv 11
rs398124146 0.742 0.360 16 3738617 missense variant G/A;C snv 12
rs747241612 0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs866987936 0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057519992 0.742 0.400 17 7674890 missense variant T/A;C;G snv 13