Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs11554495 0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 19
rs2287622 0.724 0.240 2 168973818 missense variant A/C;G;T snv 0.57 16
rs1682111 0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs2296651 0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs430397 0.763 0.240 9 125238840 intron variant C/T snv 9.1E-02 0.11 9
rs2234671 0.807 0.240 2 218164385 missense variant C/G snv 9.1E-02 0.11 7
rs26907 0.882 0.240 5 81069496 intron variant G/A;T snv 3
rs510432 0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs843720 0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs2071746 0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs1041740 0.807 0.320 21 31667849 intron variant C/T snv 0.24 8
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs28934571 0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs7080536 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs1275561861 0.672 0.360 6 29944350 missense variant G/A snv 23
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs2229113 0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35