Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7854303 1.000 0.200 9 5557672 missense variant T/C snv 1.00 1.00 1
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs9260997 1.000 0.200 6 29995539 upstream gene variant T/C snv 0.90 1
rs4857037 1.000 0.200 3 93908968 intron variant G/A snv 0.89 1
rs1048709 0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs855873 1.000 0.200 1 159077922 intron variant A/G snv 0.84 1
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs3093953 1.000 0.200 6 31506911 intron variant T/G snv 0.80 1
rs9517668 1.000 0.200 13 99271586 intron variant T/A snv 0.80 1
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs947474 0.827 0.440 10 6348488 intron variant G/A snv 0.79 5
rs2058660 0.882 0.280 2 102437989 intron variant G/A snv 0.78 4
rs1234313 0.807 0.400 1 173197108 intron variant A/G snv 0.72 6
rs2474619 0.882 0.360 6 90170316 intron variant C/A snv 0.72 3
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs1462891 1.000 0.200 8 31973417 intron variant T/C snv 0.72 1
rs1518111 0.790 0.360 1 206771300 intron variant T/C snv 0.71 9
rs27044 0.827 0.240 5 96783148 missense variant G/C snv 0.69 0.71 5
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs224127 1.000 0.200 10 62701513 intron variant A/G snv 0.69 1
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs9517723 0.925 0.200 13 99432425 non coding transcript exon variant T/C snv 0.65 2