Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs669260 0.851 0.080 9 32503442 intron variant T/A;C snv 4
rs3205166 0.925 0.040 9 32459452 synonymous variant T/A;G snv 0.35 2