Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
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
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
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs187084 0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 17
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
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
rs3764880 0.752 0.320 X 12906707 start lost A/G snv 0.31 0.30 11
rs9461776 0.763 0.240 6 32607958 intergenic variant A/G snv 8.8E-02 11
rs1799987 0.763 0.200 3 46370444 intron variant A/G snv 0.49 10
rs3021097 0.752 0.440 1 206773289 5 prime UTR variant A/G snv 10
rs4374383 0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs1993116 0.827 0.200 11 14888688 intron variant A/G snv 0.65 8
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 8
rs5930 0.827 0.200 19 11113589 synonymous variant A/G snv 0.63 0.66 8