Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs5744680 0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs198851 6 26104404 downstream gene variant T/A;C;G snv 11
rs603424 1.000 0.080 10 100315722 intron variant G/A snv 0.34 10
rs62434129 6 150687701 intron variant A/G;T snv 8.8E-02 6
rs1126930 12 49005349 missense variant G/C snv 2.1E-02 2.1E-02 5
rs11774829 8 104966140 intron variant T/A snv 7.6E-02 3
rs2761436 1 207746403 intergenic variant C/A;T snv 3