Gene entry
CELSR2
cadherin EGF LAG seven-pass G-type receptor 2
- Chromosome
- 1
- Cytoband
- 1p13.3
- Variants (rsID)
- 25
CELSR2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p13.3). Its official name is “cadherin EGF LAG seven-pass G-type receptor 2”. The reference table lists 25 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs74113801Benignmissense_variant
- rs202022169Uncertain significancesingle nucleotide variant
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.
