Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1801275 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 58
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs2308321 0.653 0.480 10 129766800 missense variant A/G snv 9.3E-02 8.7E-02 29
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs3787016 0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs55705857 0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 16
rs1412829 0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs3791679 0.925 0.120 2 55869757 intron variant A/G snv 0.20 11
rs7904519 0.763 0.240 10 113014168 intron variant A/G snv 0.55 9
rs7049105 0.807 0.120 9 22028802 intron variant A/G snv 0.58 7
rs1373481065 0.827 0.040 1 67687668 missense variant A/G snv 4.0E-06 6
rs2234248 0.827 0.040 6 41163980 upstream gene variant A/G snv 2.2E-03 5
rs11506105 0.851 0.160 7 55152484 intron variant A/G snv 0.59 4
rs12230172 0.882 0.040 12 75848895 intron variant A/G snv 0.48 4
rs723527 0.882 0.040 7 55067179 intron variant A/G snv 0.53 4
rs6470745 0.882 0.040 8 129629675 intron variant A/G snv 0.18 3
rs8105767 0.882 0.120 19 22032639 non coding transcript exon variant A/G snv 0.35 3
rs11163687 1.000 0.040 1 83199436 intergenic variant A/G snv 9.6E-02 2
rs12723208 1.000 0.040 1 211337552 intron variant A/G snv 0.13 2
rs1582417 0.925 0.040 5 160470494 intron variant A/G snv 0.80 2
rs34988193 1.000 0.040 15 64943580 missense variant A/G snv 0.31 0.28 2
rs61757955 1.000 0.040 17 75318086 3 prime UTR variant A/G snv 4.2E-02 2