Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs2494752 0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs3783553 0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs1143633 0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs3807987 0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17
rs10116253 0.851 0.120 9 117702042 upstream gene variant T/C snv 0.28 4
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1057317 0.827 0.160 9 117715764 3 prime UTR variant C/A snv 5
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83