Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs2074755 0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 17