Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9368222 1.000 0.080 6 20686765 intron variant C/A;T snv 5
rs2206734 0.882 0.160 6 20694653 intron variant C/T snv 0.20 3
rs9356744 0.882 0.120 6 20685255 intron variant T/C snv 0.42 3