| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1262765773 | 1.000 | 0.080 | 12 | 64485493 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs201970436 | 1.000 | 12 | 64481945 | missense variant | C/A | snv | 3.1E-04 | 1.7E-04 | 1 | ||
| rs758357594 | 1.000 | 12 | 64484380 | missense variant | G/A | snv | 2.0E-05 | 1 | |||
| rs1366668789 | 1.000 | 12 | 64464419 | missense variant | A/G | snv | 4.0E-06 | 2.1E-05 | 1 | ||
| rs770942184 | 1.000 | 12 | 64481943 | missense variant | T/C | snv | 2.0E-05 | 1 | |||
| rs765035140 | 1.000 | 12 | 64495767 | missense variant | C/T | snv | 1 | ||||
| rs1010930015 | 1.000 | 0.040 | 12 | 64460250 | missense variant | A/C | snv | 4.2E-06 | 1 | ||
| rs1555203557 | 12 | 64474308 | missense variant | A/G | snv | 1 | |||||
| rs1555202947 | 1.000 | 0.040 | 12 | 64467018 | missense variant | G/C | snv | 1 |