Gene entry
CDHR1
cadherin related family member 1
- Chromosome
- 10
- Cytoband
- 10q23.1
- Variants (rsID)
- 23
CDHR1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 10 (region 10q23.1). Its official name is “cadherin related family member 1”. The reference table lists 23 variants (rsID) for this gene.
Clinically classified variants
7 reference-table entries with clinical significance.
- rs45584033Benignsingle nucleotide variantCone-Rod Dystrophy, Recessive
- rs11593005Conflicting interpretationssingle nucleotide variantCone-Rod Dystrophy, Recessive
- rs137876961Conflicting interpretationssingle nucleotide variantCone-rod dystrophy 15
- rs138182270Conflicting interpretationssingle nucleotide variantCone-rod dystrophy 15
- rs140621272Conflicting interpretationssingle nucleotide variantCone-Rod Dystrophy, Recessive|Cone-rod dystrophy 15
- rs147346345Conflicting interpretationssingle nucleotide variantCone-Rod Dystrophy, Recessive|Cone-rod dystrophy 15|Retinal dystrophy|Retinitis pigmentosa
- rs192282380Uncertain 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.