Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13382811 0.882 0.040 2 144466053 intron variant C/T snv 0.21 4
rs4373767 0.882 0.040 1 219586340 regulatory region variant C/T snv 0.32 4
rs7839488 0.882 0.040 8 120550178 intron variant G/A snv 0.47 4