Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3748960 0.925 0.040 2 211383109 3 prime UTR variant C/T snv 0.96 2
rs4819554 0.776 0.320 22 17084145 upstream gene variant G/A snv 0.84 10
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 4
rs1595065 0.925 0.040 2 211377916 3 prime UTR variant G/A snv 0.73 2
rs7311358 0.827 0.160 12 20862826 missense variant G/A snv 0.81 0.72 6
rs6026584 0.925 0.040 20 58894018 intron variant T/C snv 0.70 3
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs9943582 0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs1739843 0.882 0.040 1 16016759 intron variant T/C snv 0.62 4
rs9909004 0.925 0.040 17 66310015 intron variant C/T snv 0.59 2
rs9303504 0.925 0.040 17 66319248 intron variant G/C snv 0.59 2
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs4898 0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1805126 0.925 0.040 3 38550915 synonymous variant A/G snv 0.39 0.44 2
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs740363 0.851 0.080 10 116816095 intron variant G/A snv 0.40 5
rs1799998 0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs2149954 0.882 0.080 5 158393594 intron variant C/T snv 0.37 5
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188