Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs12970291 0.763 0.120 18 75305279 intergenic variant G/A snv 2.8E-02 12