Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4759314 0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs2494752 0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs1520220 0.807 0.280 12 102402744 intron variant G/C;T snv 0.76 9
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
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
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 53
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 70
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 107
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 118
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 13
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 81
rs238406 0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 24
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 131
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 91
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs1380576 0.763 0.240 1 204519150 intron variant G/C snv 0.57 10
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 45
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 73