Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs1057519884 0.752 0.240 16 3738616 missense variant C/A;T 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
rs759610249 0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs866987936 0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 16
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 18
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs1057519917 0.807 0.160 1 11124517 missense variant A/G;T snv 7
rs587777894 0.776 0.240 1 11124516 missense variant G/A;T snv 9
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
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
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 9
rs1057519942 0.724 0.320 3 179203760 missense variant G/A snv 15
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
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 20
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 14