Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs3024971 0.827 0.200 12 57099944 intron variant T/G snv 7.8E-02 7.9E-02 7
rs4282438 0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 6
rs2516448 0.827 0.120 6 31422633 intron variant T/C;G snv 10
rs3218896 0.807 0.160 2 102015190 intron variant T/C;G snv 6
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs2043556 0.716 0.440 10 51299646 non coding transcript exon variant T/C snv 0.25 0.24 17
rs1126497 0.716 0.200 2 47373967 missense variant T/C snv 0.51 0.58 14
rs11674595 0.763 0.200 2 101994530 intron variant T/C snv 0.22 13
rs833070 0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58 11
rs7372209 0.807 0.160 3 37969217 intron variant T/C snv 0.77 7
rs1292037 0.827 0.200 17 59841547 3 prime UTR variant T/C snv 0.18 6
rs2255336 0.827 0.200 12 10379727 missense variant T/C snv 0.81 0.74 5
rs2290907 0.882 0.080 17 78097596 intron variant T/C snv 0.23 4
rs746700511 0.851 0.080 22 37665657 missense variant T/C snv 4.0E-06 4
rs1195571 0.882 0.080 12 130739483 intergenic variant T/C snv 0.97 3