Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 12
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 14
rs1057519939 0.776 0.160 3 179203763 missense variant A/C snv 10
rs1057519938 0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 11
rs121913272 0.752 0.400 3 179210192 missense variant T/C;G snv 13
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
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
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 23
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs121913281 0.623 0.520 3 179234296 missense variant C/T snv 37
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs80357382 0.763 0.240 17 43106457 missense variant T/C snv 4.0E-06 11
rs1057519946 0.732 0.280 19 52212729 missense variant C/G;T snv 18
rs1057519947 0.790 0.160 19 52212730 missense variant G/A snv 9
rs121913496 0.724 0.440 11 533873 missense variant C/A;G;T snv 16
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 37
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73