Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs2234767 0.649 0.280 10 88989499 intron variant G/A;T snv 0.15 30
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs143383 0.724 0.320 20 35438203 5 prime UTR variant G/A snv 0.47 17
rs1800012 0.763 0.320 17 50200388 intron variant C/A snv 0.14 13
rs2073711 0.807 0.160 15 65201874 missense variant A/G snv 0.56 0.61 7
rs5030772 0.790 0.320 1 172664210 intron variant A/G snv 9.9E-02 7
rs77245812 0.882 0.040 2 20003169 missense variant G/A snv 1.5E-02 1.2E-02 3
rs2276454 0.925 0.040 12 47982508 synonymous variant G/A snv 0.39 0.38 2