Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs621559 0.827 0.080 1 43179740 intron variant G/A snv 0.18 5
rs6489769 0.851 0.120 12 963799 intron variant C/A;T snv 4
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs72554204 0.827 0.120 19 43546062 missense variant C/T snv 1.2E-04 1.3E-04 5
rs7963551 0.807 0.160 12 912349 3 prime UTR variant T/G snv 0.13 7
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs9288516 0.827 0.120 2 216188541 intron variant T/A snv 5.0E-02 6