Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 5
rs7512552 1.000 0.120 1 150293284 upstream gene variant T/C snv 0.63 4
rs1295686 0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 3
rs3091307 0.925 0.160 5 132653444 intron variant A/G snv 0.34 2