Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7697932 | 1.000 | 0.120 | 4 | 100084161 | intron variant | A/G | snv | 0.72 | 1 | ||
rs4804368 | 1.000 | 0.120 | 19 | 7190279 | intron variant | A/G;T | snv | 1 | |||
rs234043 | 1.000 | 0.120 | 3 | 172595577 | non coding transcript exon variant | T/C | snv | 0.74 | 1 | ||
rs11637556 | 1.000 | 0.120 | 15 | 66436613 | intron variant | A/C;G | snv | 1 | |||
rs4662750 | 1.000 | 0.120 | 2 | 127634972 | non coding transcript exon variant | A/C | snv | 0.69 | 1 | ||
rs10054504 | 1.000 | 0.120 | 5 | 32000377 | intron variant | T/A;C | snv | 1 | |||
rs59294613 | 1.000 | 0.120 | 7 | 124914213 | intron variant | C/A | snv | 0.28 | 1 | ||
rs35252396 | 1.000 | 0.120 | 8 | 127877125 | intron variant | AC/CG | mnv | 1 | |||
rs6470588 | 1.000 | 0.120 | 8 | 127877125 | intron variant | A/C | snv | 0.53 | 1 | ||
rs6470589 | 1.000 | 0.120 | 8 | 127877126 | intron variant | C/A;G | snv | 1 | |||
rs10484683 | 1.000 | 0.120 | 6 | 147830941 | intron variant | A/G | snv | 0.18 | 1 | ||
rs13027293 | 1.000 | 0.120 | 2 | 119243542 | intron variant | G/T | snv | 0.33 | 1 | ||
rs2203002 | 1.000 | 0.120 | 3 | 142077397 | intron variant | C/T | snv | 6.4E-02 | 1 | ||
rs12105521 | 1.000 | 0.120 | 2 | 144450769 | intron variant | G/A;T | snv | 1 | |||
rs12105918 | 1.000 | 0.120 | 2 | 144450626 | intron variant | T/C | snv | 6.1E-02 | 1 | ||
rs13401103 | 1.000 | 0.120 | 2 | 144441056 | intron variant | G/A;T | snv | 1 | |||
rs72858474 | 1.000 | 0.120 | 2 | 144441322 | intron variant | G/A | snv | 6.2E-02 | 1 | ||
rs72858496 | 1.000 | 0.120 | 2 | 144452349 | intron variant | C/T | snv | 5.9E-02 | 1 | ||
rs11813268 | 0.925 | 0.120 | 10 | 103922538 | upstream gene variant | C/T | snv | 0.31 | 2 | ||
rs1417080 | 0.925 | 0.120 | 9 | 79515946 | non coding transcript exon variant | T/C | snv | 0.35 | 2 | ||
rs3118523 | 0.925 | 0.120 | 9 | 134443675 | downstream gene variant | G/A | snv | 0.75 | 2 | ||
rs6466135 | 0.925 | 0.120 | 7 | 106861053 | upstream gene variant | A/G | snv | 0.71 | 2 | ||
rs7132434 | 0.925 | 0.120 | 12 | 26319629 | non coding transcript exon variant | A/G | snv | 0.62 | 2 | ||
rs748964 | 0.925 | 0.120 | 9 | 134442243 | downstream gene variant | C/G;T | snv | 2 | |||
rs1154454 | 0.925 | 0.120 | 4 | 99417185 | intron variant | A/G | snv | 0.22 | 2 |