Gene entry
GRHL2
grainyhead like transcription factor 2
- Chromosome
- 8
- Cytoband
- 8q22.3
- Variants (rsID)
- 46
GRHL2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 8 (region 8q22.3). Its official name is “grainyhead like transcription factor 2”. The reference table lists 46 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs3779617Benignsingle nucleotide variant
Other listed variants
- rs471757
- rs479690
- rs496887
- rs515743
- rs548650
- rs608337
- rs608799
- rs642074
- rs667737
- rs812890
- rs1892754
- rs2127035
- rs3735717
- rs3956241
- rs6980991
- rs6988306
- rs7010796
- rs7838699
- rs9297306
- rs9642972
- rs10099482
- rs10955258
- rs11994981
- rs12679638
- rs16867810
- rs16868134
- rs17477680
- rs35477966
- rs35526650
- rs57874832
- rs61627948
- rs62519115
- rs72674236
- rs72674248
- rs72674257
- rs72674259
- rs73277298
- rs73279201
- rs73701911
- rs75279991
- rs76758854
- rs78423496
- rs111838256
- rs117511140
- rs117937767
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.