Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs79105258 12 111280427 intron variant C/A;T snv 24
rs597808 0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs198851 6 26104404 downstream gene variant T/A;C;G snv 15
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 10
rs10766533 11 19203130 intron variant T/A snv 0.62 4
rs12693982 2 203220912 intron variant C/T snv 0.38 3