Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs121913254 0.658 0.440 1 114713909 stop gained G/A;C;T snv 31
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs879253942 0.677 0.400 17 7673826 missense variant A/G snv 28
rs121434596 0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 26
rs5743618 0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 25
rs4148323 0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 22
rs776746 0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs2069837 0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs121913238 0.732 0.240 12 25227343 missense variant G/C;T snv 17
rs3757441 0.752 0.200 7 148827660 intron variant C/T snv 0.80 12
rs762513613 0.752 0.280 1 161591315 missense variant A/G snv 4.2E-06 7.4E-06 11
rs1053004 0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11
rs3853839 0.752 0.480 X 12889539 3 prime UTR variant C/G;T snv 10