Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057519941 0.776 0.240 3 179203761 missense variant T/C;G snv 10
rs1057519942 0.724 0.320 3 179203760 missense variant G/A snv 16
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913283 0.724 0.440 3 179234286 missense variant G/A;T snv 4.0E-06 16
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 11
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 12
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 14
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 41
rs121909229 0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32