Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs629849 0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 8
rs2994809 1 119809354 intron variant T/C snv 0.91 1
rs629367 0.776 0.200 11 122146306 intron variant C/A snv 0.88 11
rs723526 1.000 7 55067126 intron variant A/G snv 0.86 2
rs2494752 0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs3775292 0.851 0.080 4 186081871 non coding transcript exon variant C/G snv 0.82 5
rs7034162 0.882 0.040 9 14190288 intron variant A/T snv 0.81 4
rs2221903 0.752 0.360 4 122617757 intron variant C/T snv 0.77 12
rs1570360 0.641 0.680 6 43770093 upstream gene variant A/G snv 0.76 38
rs4946728 1.000 0.120 6 106142488 intron variant A/C snv 0.72 3
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs373572 0.882 0.120 3 8913705 missense variant C/T snv 0.68 0.70 6
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 70
rs11016879 0.882 0.040 10 129691518 intron variant A/C;G snv 0.66 4
rs3743073 0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
rs3213245 0.742 0.240 19 43575535 5 prime UTR variant G/A snv 0.65 0.60 13
rs1800544 0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 12
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 20
rs1360485 0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 15
rs514049 0.827 0.160 15 58750164 intron variant C/A snv 0.57 6
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs2119882 0.807 0.320 4 186555751 upstream gene variant T/C snv 0.57 9
rs7795743 7 55182437 non coding transcript exon variant G/A snv 0.56 1
rs3740530 1.000 0.080 10 113574365 synonymous variant C/T snv 0.63 0.55 2