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
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 18
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs560887 0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 9
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 5
rs2232326 2 168907981 missense variant T/C snv 5.1E-03 3.3E-03 3