Gene entry
NR1H3
nuclear receptor subfamily 1 group H member 3
- Chromosome
- 11
- Cytoband
- 11p11.2
- Variants (rsID)
- 9
NR1H3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 11 (region 11p11.2). Its official name is “nuclear receptor subfamily 1 group H member 3”. The reference table lists 9 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs61731956Pathogenicsingle nucleotide variantMultiple sclerosis
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.
