Gene entry
GRHL3
grainyhead like transcription factor 3
- Chromosome
- 1
- Cytoband
- 1p36.11
- Variants (rsID)
- 20
GRHL3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p36.11). Its official name is “grainyhead like transcription factor 3”. The reference table lists 20 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs41268753Benignsingle nucleotide variantVan der Woude syndrome 2
- rs6694170Benignsingle nucleotide variantVan der Woude syndrome 2
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.
