Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229 0.564 0.600 11 534289 missense variant C/A;G;T snv 52
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
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs104894228 0.605 0.560 11 534286 missense variant C/A;G;T snv 30
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
rs104894226 0.658 0.560 11 534285 missense variant C/A;G;T snv 23
rs121909229 0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 21
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 20
rs1057519981 0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs730882005 0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs753660142 0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
rs11554273 0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 17
rs747342068 0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 17
rs866775781 0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs1057519996 0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 16
rs121913495 0.672 0.400 20 58909366 missense variant G/A;T snv 15
rs1057519942 0.724 0.320 3 179203760 missense variant G/A snv 15