Gene entry
WNT7A
Wnt family member 7A
- Chromosome
- 3
- Cytoband
- 3p25.1
- Variants (rsID)
- 25
WNT7A is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p25.1). Its official name is “Wnt family member 7A”. The reference table lists 25 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs104893832Pathogenicsingle nucleotide variantFuhrmann syndrome
- rs387907231Pathogenicsingle nucleotide variantSchinzel phocomelia syndrome
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.