Overview
- Approved name
- Cytogenetic location
- -
- Locus type
- -
- In SaudiVarKB
- 4 articles, 4 mentions
4Publications2Co-reported phenotypes1Reported variants
0ClinVar pathogenic / likely pathogenic
0Saudi regions
OpenLiterature networkCo-reported phenotypes
Phenotypes named in the same articles as WNT1. Co-mention, not a proven association.
| Phenotype | Articles | Evidence |
|---|---|---|
| osteogenesis imperfecta | 3 | View sentences |
| developmental delay | 1 | View sentences |
Reported variants
Variants linked to WNT1 through dbSNP or LitVar2. ClinVar status is shown for core-subset variants.
| Variant | rsID | Articles | ClinVar |
|---|---|---|---|
| rs387907358 | rs387907358 | 1 | - |
Saudi regions
Regions or cities named in the abstracts of articles that mention WNT1.
No Saudi region named.