Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9277458 0.925 0.200 6 33085390 intron variant A/C;T snv 2
rs9357156 1.000 0.080 6 33073296 intron variant A/C;T snv 1
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs12252 0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 23
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs9808753 0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs2070959 0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 16
rs3077 0.701 0.440 6 33065245 3 prime UTR variant A/G snv 0.29 16
rs4804803 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs5744174 0.742 0.360 1 223111186 missense variant A/G snv 0.39 0.34 13
rs9277535 0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs2834167 0.752 0.360 21 33268483 missense variant A/G snv 0.33 0.25 11
rs3093059
CRP
0.752 0.520 1 159715346 upstream gene variant A/G snv 0.13 11
rs3754093 0.776 0.240 1 241846814 upstream gene variant A/G snv 0.23 11
rs1046282 0.776 0.160 19 45407414 3 prime UTR variant A/G snv 0.30 10