| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11920090 | 1.000 | 0.040 | 3 | 170999732 | intron variant | T/A | snv | 0.20 | 3 | ||
| rs3138708 | 3 | 171009914 | intron variant | T/G | snv | 3.1E-02 | 2 | ||||
| rs5394 | 3 | 171027104 | intron variant | G/A | snv | 0.15 | 2 | ||||
| rs10513686 | 3 | 171007753 | intron variant | G/A | snv | 0.21 | 1 |