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
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
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
rs461404 0.925 0.080 5 40799438 upstream gene variant G/A snv 0.70 3
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs154268 0.925 0.080 5 40795766 intron variant C/T snv 0.69 3
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs4796030 0.827 0.120 17 35003131 3 prime UTR variant A/C snv 0.66 6
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs3743073 0.807 0.120 15 78617197 intron variant G/T snv 0.61 11
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
rs2172362 0.925 0.080 1 39829228 intergenic variant T/C snv 0.58 3
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1342387 0.776 0.120 1 202945228 intron variant T/C snv 0.53 12
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs2735940 0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 25
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131