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 81
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs4240624 0.882 0.040 8 9326721 intron variant G/A snv 0.87 5
rs12784396 0.925 0.040 10 100267650 5 prime UTR variant C/A;T snv 4