Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs79184941 0.617 0.600 10 121520163 missense variant G/A;C snv 5.6E-05; 4.0E-06 41
rs121913400 0.683 0.360 3 41224610 missense variant C/A;G;T snv 26
rs121913478 0.708 0.640 10 121515280 missense variant T/C snv 17
rs4430796 0.790 0.280 17 37738049 intron variant A/G snv 0.52 14
rs12970291 0.763 0.120 18 75305279 intergenic variant G/A snv 2.8E-02 12
rs1057519854 0.882 0.080 10 121488063 missense variant A/T snv 7
rs11263763 0.882 0.200 17 37743574 intron variant A/G snv 0.43 6