| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1815739 | 0.763 | 0.240 | 11 | 66560624 | stop gained | C/T | snv | 0.37 | 17 | ||
| rs1799865 | 1.000 | 0.040 | 3 | 46358307 | synonymous variant | T/C | snv | 0.32 | 0.32 | 2 | |
| rs1277121650 | 5 | 96746364 | missense variant | T/C | snv | 7.0E-06 | 1 | ||||
| rs1355799280 | 5 | 96742749 | missense variant | T/C | snv | 7.0E-06 | 1 | ||||
| rs750877321 | 5 | 96741291 | missense variant | T/C | snv | 1.2E-05 | 1 | ||||
| rs774652019 | 5 | 96765222 | splice acceptor variant | A/G;T | snv | 8.1E-06 | 1 | ||||
| rs3918358 | 3 | 46352928 | upstream gene variant | C/A | snv | 0.68 | 1 | ||||
| rs779255105 | 5 | 96762316 | missense variant | G/A | snv | 4.0E-06 | 1 |