Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2681492 0.925 0.040 12 89619312 intron variant T/C;G snv 7
rs2681472 0.882 0.080 12 89615182 intron variant A/G snv 0.14 6
rs57481061 1.000 0.040 12 89625401 intron variant C/G snv 0.14 1