| Approved symbol | RNASEH2A |
|---|---|
| Approved name | ribonuclease H2 subunit A |
| HGCN ID | HGNC:18518 |
| Previous symbols | |
| Inheritance | |
| OMIM | 606034 |
| Chromosome | 19p13.13 |
| Panel(s) |
NGS Dementia/ALS NGS Epilepsy NGS Intellectual disability NGS Mendeliome NGS Movement disorders NGS Preconception panel (for consanguineous couples) NGS Primary immunodeficiency PID NGS White matter disease RNASEH2A Analysis |
