Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4149056 0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs11045879 1.000 0.120 12 21229685 intron variant T/C snv 0.18 4