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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.