Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs4647958 0.851 0.080 20 49984094 missense variant T/C snv 0.18 0.29 5
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs712 0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs931127 0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs1360485 0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 16
rs3213245 0.742 0.240 19 43575535 5 prime UTR variant G/A snv 0.65 0.60 13
rs3743073 0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs629367 0.776 0.200 11 122146306 intron variant C/A snv 0.88 11