Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs1532085 0.882 0.080 15 58391167 intron variant A/G;T snv 7
rs6511720 0.790 0.120 19 11091630 intron variant G/T snv 0.12 7
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 7