Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs17886084 1.000 0.080 11 102799765 intron variant C/- delins 2
rs5496 1.000 0.080 19 10284771 intron variant G/A snv 7.8E-03 3.3E-02 1
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs14158 0.851 0.160 19 11131368 synonymous variant G/A snv 0.24 0.22 5
rs4374383 0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs3741981 0.882 0.120 12 112911065 missense variant G/A;C snv 3
rs10774671 0.732 0.480 12 112919388 splice acceptor variant G/A;C snv 0.67 14
rs7080536 0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs236918 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs13412852 0.851 0.120 2 11774815 intron variant C/T snv 0.26 4
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs9402373 1.000 0.080 6 131956291 intron variant C/A;G;T snv 1
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs10833 0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs16851720 0.827 0.120 3 141744456 intron variant A/C snv 0.21 5
rs12075 0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs17047200 0.827 0.200 4 166008836 intron variant A/T snv 0.18 5