| Approved symbol | TREM2 |
|---|---|
| Approved name | triggering receptor expressed on myeloid cells 2 |
| HGCN ID | HGNC:17761 |
| Previous symbols | |
| Inheritance | |
| OMIM | 605086 |
| Chromosome | 6p21.1 |
| Panel(s) |
NGS Amyotrophic lateral sclerosis ALS NGS Dementia risk factors NGS Mendeliome NGS Movement disorders NGS Preconception panel (for consanguineous couples) NGS Skeletal Dysplasia NGS White matter disease |
