Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3814113 | 0.827 | 0.200 | 9 | 16915023 | upstream gene variant | T/C | snv | 0.41 | 2 | ||
rs1192691 | 0.925 | 0.120 | 10 | 36880367 | regulatory region variant | G/T | snv | 0.90 | 1 | ||
rs142091544 | 0.925 | 0.120 | 5 | 168286995 | upstream gene variant | C/T | snv | 2.1E-02 | 1 | ||
rs1574560 | 1.000 | 0.120 | 3 | 166329716 | intergenic variant | T/C | snv | 0.42 | 1 | ||
rs1614627 | 1.000 | 0.120 | 1 | 20620263 | downstream gene variant | A/C | snv | 0.86 | 1 | ||
rs2660753 | 0.790 | 0.240 | 3 | 87061524 | intergenic variant | T/C | snv | 0.76 | 1 | ||
rs4286604 | 0.925 | 0.120 | 4 | 69576447 | intron variant | A/G | snv | 0.76 | 1 | ||
rs633862 | 0.925 | 0.120 | 9 | 133279871 | upstream gene variant | T/C | snv | 0.49 | 1 | ||
rs7230264 | 1.000 | 0.120 | 18 | 27347470 | intron variant | G/A | snv | 0.15 | 1 | ||
rs7748275 | 0.882 | 0.120 | 6 | 3580855 | downstream gene variant | T/A | snv | 8.2E-02 | 1 | ||
rs8044477 | 1.000 | 0.120 | 16 | 58942687 | intron variant | A/G | snv | 0.53 | 1 | ||
rs9283636 | 1.000 | 0.120 | 3 | 166315136 | intergenic variant | G/A | snv | 0.46 | 1 | ||
rs9787692 | 1.000 | 0.120 | 10 | 8603200 | intergenic variant | T/G | snv | 0.30 | 1 | ||
rs8170 | 0.724 | 0.160 | 19 | 17278895 | synonymous variant | G/A | snv | 0.15 | 0.18 | 3 | |
rs11782652 | 0.851 | 0.120 | 8 | 81741409 | intron variant | A/G | snv | 6.6E-02 | 2 | ||
rs1413299 | 0.925 | 0.120 | 9 | 98998959 | intron variant | G/A;T | snv | 1 | |||
rs2070074 | 0.742 | 0.360 | 9 | 34649445 | missense variant | A/G | snv | 9.2E-02 | 7.4E-02 | 1 | |
rs115344852 | 1.000 | 0.120 | 6 | 28518321 | intron variant | A/C | snv | 1 | |||
rs1695 | 0.457 | 0.880 | 11 | 67585218 | missense variant | A/G | snv | 0.34 | 0.36 | 1 | |
rs2072590 | 0.851 | 0.120 | 2 | 176177905 | non coding transcript exon variant | A/C;T | snv | 2 | |||
rs11651755 | 0.763 | 0.160 | 17 | 37739849 | intron variant | T/C | snv | 0.52 | 4 | ||
rs7405776 | 0.807 | 0.120 | 17 | 37733029 | intron variant | G/A;C | snv | 3 | |||
rs757210 | 0.807 | 0.160 | 17 | 37736525 | intron variant | C/G;T | snv | 2 | |||
rs5498 | 0.531 | 0.760 | 19 | 10285007 | missense variant | A/G | snv | 0.44 | 0.37 | 2 | |
rs1834481 | 0.882 | 0.160 | 11 | 112153104 | non coding transcript exon variant | C/G | snv | 0.16 | 1 |