Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs61816761 0.658 0.640 1 152313385 stop gained G/A;T snv 9.4E-03; 8.0E-06 43
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs2305480 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 10
rs4794820 0.790 0.160 17 39933091 intron variant A/G;T snv 9
rs928413 0.807 0.120 9 6213387 upstream gene variant G/A;C snv 7
rs1558641 0.925 0.080 2 102149405 intron variant G/A snv 0.13 3