Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8068952 1.000 0.040 17 61209283 intron variant G/C snv 0.60 2
rs1476098 1.000 0.040 17 61159652 intron variant A/C snv 0.66 1
rs7212798 1.000 0.040 17 60936127 intron variant T/A;C snv 1
rs8079951 1.000 0.040 17 61165403 intron variant T/A snv 0.68 1
rs8080784 1.000 0.040 17 60939664 intron variant T/C snv 0.22 1