Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 15
rs587781288 0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs876659802 0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs1057519977 0.763 0.360 17 7675189 missense variant G/C snv 13
rs876660333 0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519978 0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs121913338 0.677 0.400 7 140753354 missense variant T/A;C;G snv 12
rs1057519933 0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519934 0.790 0.240 3 179199158 missense variant G/C snv 11
rs1057519935 0.790 0.240 3 179199157 missense variant A/G snv 11
rs397516896 0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs1023835002 0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519877 0.763 0.280 15 44711549 start lost G/A snv 10
rs1057519879 0.763 0.280 15 44711548 start lost T/C;G snv 10
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs121913502 0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 6
rs267606870 0.763 0.280 15 90088703 missense variant G/A;C snv 6