Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs3024490 0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs3021097 0.752 0.440 1 206773289 5 prime UTR variant A/G snv 10
rs1518111 0.790 0.360 1 206771300 intron variant T/C snv 0.71 9
rs3024493 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 9
rs3021094 0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 8
rs3024498 0.790 0.360 1 206768184 3 prime UTR variant T/C snv 0.20 7
rs1554286 0.790 0.320 1 206770888 5 prime UTR variant A/G;T snv 0.72 7
rs3024496 0.827 0.200 1 206768519 3 prime UTR variant A/G snv 0.43 6
rs1518110 0.851 0.160 1 206771516 intron variant A/C;T snv 5
rs2222202 0.827 0.160 1 206772036 intron variant G/A snv 0.39 5
rs1878672 0.882 0.080 1 206770368 intron variant G/A;C;T snv 3
rs3790622 0.882 0.320 1 206771818 intron variant G/A snv 1.5E-03 3
rs3024491 0.925 0.040 1 206771701 intron variant C/A;T snv 2
rs1373589952 1.000 0.120 1 206772296 missense variant G/A snv 7.0E-06 1
rs145922845 1.000 0.040 1 206772393 missense variant C/T snv 1.9E-03 1.8E-03 1
rs1800893 1.000 0.120 1 206773822 intron variant C/T snv 0.41 1
rs3024492 1 206770767 5 prime UTR variant T/A snv 0.17 1
rs3024495 1.000 0.080 1 206769068 intron variant C/A;T snv 1