Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs1899663 0.683 0.280 12 53967210 intron variant C/A snv 0.28 22
rs4081134 0.790 0.160 14 100855451 non coding transcript exon variant G/A snv 0.29 7
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs34330 0.724 0.280 12 12717761 5 prime UTR variant T/C snv 0.70 14