Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4821480 0.807 0.160 22 36299201 intron variant G/T snv 0.78 9
rs104894833 0.776 0.280 X 101403984 missense variant C/G snv 1.2E-04 1.9E-05 11