Source: GWASCAT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10250602 | 7 | 23264082 | intron variant | T/C | snv | 0.35 | 1 | ||||
| rs10262243 | 7 | 23251368 | intron variant | G/A | snv | 0.37 | 1 | ||||
| rs2268748 | 7 | 23273552 | synonymous variant | T/C | snv | 0.11 | 5.5E-02 | 1 | |||
| rs28458177 | 7 | 23255253 | intron variant | G/A | snv | 0.36 | 1 | ||||
| rs858240 | 7 | 23244618 | intron variant | A/G | snv | 0.54 | 1 |