Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28935197 0.776 0.280 X 101398942 missense variant T/C snv 5.5E-06 10
rs148158093 0.925 0.200 X 101403828 missense variant G/A snv 2.2E-04 4.0E-04 3
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs17132261 1.000 0.080 5 110672513 intron variant C/T snv 4.8E-02 2
rs1436109 1.000 0.080 11 113120896 intron variant G/T snv 8.5E-02 3
rs1801252 0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs5068 0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs2073618 0.716 0.480 8 118951813 missense variant G/C snv 0.52 0.60 19
rs1050606 1.000 0.080 4 121696891 5 prime UTR variant A/C snv 0.50 2
rs9402349 1.000 0.080 6 131863968 intron variant A/C snv 9.8E-02 1
rs1974201 1.000 0.080 6 131889981 intron variant G/A;C;T snv 1
rs17168525 1.000 0.080 7 135928514 3 prime UTR variant G/A snv 1.4E-02 1
rs5029939 0.701 0.440 6 137874586 intron variant C/G snv 0.13 19
rs1799998 0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs5522 0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs2070951 0.776 0.320 4 148436862 splice region variant G/A;C snv 4.2E-06; 0.53 9
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1800888 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2074192 0.827 0.160 X 15564667 intron variant C/T snv 0.40 9
rs869312687 0.925 0.080 1 155910695 missense variant T/G snv 8