Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1214285376 0.776 0.200 19 43543490 missense variant G/T snv 4.0E-06 8
rs148611340 0.790 0.120 19 43543621 missense variant G/A;C snv 4.0E-06; 1.2E-05 7
rs199613843 0.807 0.160 19 43551609 synonymous variant C/T snv 4.0E-06 7.0E-06 6
rs7963551 0.807 0.160 12 912349 3 prime UTR variant T/G snv 0.13 7
rs2307191 0.827 0.120 19 43553616 missense variant G/A snv 1.2E-03 4.8E-03 5
rs621559 0.827 0.080 1 43179740 intron variant G/A snv 0.18 5
rs72554204 0.827 0.120 19 43546062 missense variant C/T snv 1.2E-04 1.3E-04 5
rs9288516 0.827 0.120 2 216188541 intron variant T/A snv 5.0E-02 6
rs25490 0.851 0.120 19 43552189 missense variant T/C snv 7.2E-03 2.6E-02 4
rs6489769 0.851 0.120 12 963799 intron variant C/A;T snv 4
rs17006625 0.925 0.080 3 20119604 missense variant A/C;G snv 4.0E-06; 3.3E-02 3