Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 25
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs6505162 0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs4898 0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs2227982 0.677 0.480 2 241851281 missense variant G/A snv 9.2E-02 4.3E-02 24
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs698 0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs10204525 0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs11554495 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 19
rs2596542 0.724 0.200 6 31398818 upstream gene variant C/T snv 0.41 18
rs7096206 0.708 0.480 10 52771925 upstream gene variant G/A;C;T snv 17
rs4804803 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs4149117 0.763 0.360 12 20858546 missense variant T/C;G snv 0.81 15
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs17580 0.776 0.160 14 94380925 missense variant T/A snv 2.3E-02 2.9E-02 14
rs2296651 0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs9514828 0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs1053004 0.776 0.280 17 42314074 3 prime UTR variant G/A snv 0.48 11
rs75961395 0.763 0.280 7 117509123 missense variant G/A;T snv 4.0E-05 10