| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs939336 | 0.925 | 0.040 | 3 | 183967746 | stop gained | A/G;T | snv | 0.58 | 2 | ||
| rs1132776 | 0.925 | 0.040 | 3 | 183978614 | synonymous variant | A/G | snv | 0.58 | 0.61 | 2 | |
| rs1459206697 | 1.000 | 0.080 | 3 | 183961651 | missense variant | G/C | snv | 4.0E-06 | 1 | ||
| rs10937158 | 3 | 183990651 | intron variant | T/C | snv | 0.62 | 1 | ||||
| rs3749438 | 3 | 183987396 | 3 prime UTR variant | G/A | snv | 0.33 | 1 |