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 |