Gene entry
RORC
RAR related orphan receptor C
- Chromosome
- 1
- Cytoband
- 1q21.3
- Variants (rsID)
- 10
RORC is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q21.3). Its official name is “RAR related orphan receptor C”. The reference table lists 10 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs17582155Likely benignsingle nucleotide variantAutosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency
- rs142141845Uncertain significancesingle nucleotide variantAutosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency
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.