Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs651007 | 0.851 | 0.160 | 9 | 133278431 | upstream gene variant | T/A;C | snv | 22 | |||
| rs657152 | 0.882 | 0.200 | 9 | 133263862 | intron variant | A/C;T | snv | 22 | |||
| rs687621 | 0.851 | 0.240 | 9 | 133261662 | intron variant | G/A;C | snv | 18 | |||
| rs687289 | 1.000 | 0.120 | 9 | 133261703 | intron variant | A/G | snv | 15 | |||
| rs1801020 | 1.000 | 0.040 | 5 | 177409531 | 5 prime UTR variant | A/G | snv | 0.65 | 0.67 | 8 | |
| rs2731672 | 5 | 177415473 | intron variant | T/C | snv | 0.66 | 6 | ||||
| rs2545801 | 5 | 177414338 | intron variant | T/C | snv | 0.56 | 5 | ||||
| rs7447593 | 5 | 177397136 | non coding transcript exon variant | C/G;T | snv | 4 | |||||
| rs2287694 | 5 | 177433292 | intron variant | T/C | snv | 8.5E-02 | 2 |