Approved symbol | WNT1 |
---|---|
Approved name | Wnt family member 1 |
HGCN ID | HGNC:12774 |
Previous symbols | INT1 |
Inheritance | |
OMIM | 164820 |
Chromosome | 12q13.12 |
Panel(s) |
NGS Mendeliome NGS Osteogenesis imperfecta and related disorders NGS Preconception panel (for consanguineous couples) NGS Skeletal Dysplasia |