Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs210143 0.827 0.160 6 33579153 intron variant T/C snv 0.74 1
rs2285803 0.925 0.160 6 31139481 intron variant T/C snv 0.72 2
rs1672753 0.882 0.240 3 3179746 upstream gene variant C/T snv 0.71 4
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
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 81
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 4
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs4351714 1.000 0.160 1 202791530 intron variant T/C snv 0.61 1
rs1884444 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 34
rs4284505 1.000 0.160 13 91349218 non coding transcript exon variant A/G snv 0.51 1
rs711613 1.000 0.160 3 3178805 intron variant T/C snv 0.51 1
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1419881 0.851 0.280 6 31162816 3 prime UTR variant G/A snv 0.50 2
rs710190 0.925 0.200 22 39131785 3 prime UTR variant T/C snv 0.48 1
rs7336610 0.827 0.240 13 91352883 intron variant C/T snv 0.47 5
rs2151280 0.701 0.360 9 22034720 non coding transcript exon variant G/A snv 0.46 11
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs13409 1.000 0.160 6 31164363 3 prime UTR variant G/A snv 0.44 1
rs1049623 0.925 0.200 6 30897052 synonymous variant T/C snv 0.47 0.43 2
rs877529 1.000 0.160 22 39146287 intron variant G/A snv 0.43 1
rs9344 0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 30
rs12717 0.925 0.160 6 170553212 missense variant G/C snv 0.42 0.38 2
rs6465657 0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37 4
rs3087243 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 35