Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11891311 2 233730664 intron variant G/A snv 0.42 4
rs2417940 12 20864941 intron variant T/A;C snv 3
rs4148323 0.701 0.440 2 233760498 missense variant G/A snv 2.2E-02 9.2E-03 3