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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.