Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs759435862 0.925 0.080 2 8776852 missense variant C/A;T snv 2.0E-05 5
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs373572 0.882 0.120 3 8913705 missense variant C/T snv 0.68 0.70 6
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3212227 0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913444 0.724 0.160 7 55191831 missense variant T/A;C;G snv 18
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31