Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1412125 0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2221903 0.752 0.360 4 122617757 intron variant C/T snv 0.77 12
rs2285053 0.752 0.320 16 55478465 intron variant C/T snv 0.12 15
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs3756824 0.925 0.080 6 22298508 intron variant C/G;T snv 3
rs3774937 0.776 0.280 4 102513096 intron variant T/C snv 0.26 9
rs6464926 0.882 0.120 7 148821919 intron variant C/T snv 0.41 4
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs13387042 0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 16
rs4442975 0.827 0.120 2 217056046 intergenic variant G/T snv 0.47 7
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs62625308 0.851 0.200 17 43091924 stop gained G/A;C snv 1.2E-05 8
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1056123575 0.925 0.080 21 26844557 missense variant G/A snv 4.2E-06 7.0E-06 4
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1136201 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs11662595 0.882 0.120 18 24477006 missense variant A/G snv 8.6E-02 7.6E-02 7
rs1172398253 0.925 0.080 1 85582045 missense variant C/T snv 4.0E-06 4
rs1213469537 0.882 0.080 7 116559145 missense variant C/T snv 4.0E-06 1.4E-05 9