Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs2305480 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 10
rs4794820 0.790 0.160 17 39933091 intron variant A/G;T snv 9
rs569108 0.790 0.200 11 60095631 missense variant A/G snv 4.7E-02 7.3E-02 8
rs6967330 0.827 0.120 7 106018005 missense variant G/A snv 0.19 0.21 8
rs928413 0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7
rs4065275 0.807 0.160 17 39924612 intron variant A/G;T snv 0.56 6
rs6871536 0.827 0.160 5 132634182 intron variant T/C snv 0.24 5
rs10494132 0.851 0.080 1 111289601 upstream gene variant T/C snv 0.26 4
rs1999071 0.851 0.080 14 22659998 regulatory region variant T/C snv 0.29 4
rs73985228 0.882 0.080 17 39922412 3 prime UTR variant G/C;T snv 3