Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519886 0.752 0.240 3 41224609 missense variant T/A;C;G snv 11
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;T snv 17
rs121913412 0.724 0.280 3 41224633 missense variant A/C;G;T snv 10
rs121913413 0.763 0.240 3 41224634 missense variant C/A;T snv 9
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs121913233 0.627 0.520 11 533874 missense variant T/A;C;G snv 20
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 15
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 23
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs28933406 0.667 0.480 11 533875 missense variant G/C;T snv 17
rs1057519738 0.790 0.160 17 39725079 missense variant G/A snv 4.0E-06 7
rs1057519919 0.851 0.160 2 15942195 missense variant C/T snv 5
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
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
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 45
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 14
rs587777790 0.732 0.280 3 179199690 missense variant G/A snv 12
rs1057519943 0.790 0.160 12 132676598 missense variant G/C;T snv 5
rs1057519944 0.882 0.160 12 132676599 missense variant G/A snv 5