Gene entry

OR2C1

olfactory receptor family 2 subfamily C member 1

Chromosome: 16
Cytoband: 16p13.3
Variants (rsID): 1

OR2C1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 16 (region 16p13.3). Its official name is “olfactory receptor family 2 subfamily C member 1”. The reference table lists 1 variant (rsID) for this gene.

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Clinically classified variants

1 reference-table entries with clinical significance.

rs1218762Not classifiedmissense_variantAtaxia and Polyneuropathy, Adult-Onset|Autosomal Recessive Cerebellar Ataxia|Hereditary Ataxia|Spinocerebellar Ataxia, Autosomal Recessive 16|Spinocerebellar Ataxia 15

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.