Gene entry
HR
HR lysine demethylase and nuclear receptor corepressor
- Chromosome
- 8
- Cytoband
- 8p21.3
- Variants (rsID)
- 21
HR is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 8 (region 8p21.3). Its official name is “HR lysine demethylase and nuclear receptor corepressor”. The reference table lists 21 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs115643651Benignsingle nucleotide variantAlopecia universalis congenita|Atrichia with papular lesions
- rs117197822Benignsingle nucleotide variantAtrichia with papular lesions|Alopecia universalis congenita
- rs138941448Benignsingle nucleotide variantAtrichia with papular lesions|Alopecia universalis congenita
- rs7014851Benignsingle nucleotide variantAlopecia universalis congenita|Atrichia with papular lesions
- rs73549525Benignsingle nucleotide variantAtrichia with papular lesions|Alopecia universalis congenita
- rs74596676Benignsingle nucleotide variantAlopecia universalis congenita|Atrichia with papular lesions
- rs77758962Benignsingle nucleotide variantAtrichia with papular lesions|Alopecia universalis congenita
- rs112016555Likely benignsingle nucleotide variantAtrichia with papular lesions|Alopecia universalis congenita
- rs148782064Uncertain significancesingle nucleotide variantAtrichia with papular lesions|Alopecia universalis congenita
- rs151036296Uncertain significancesingle nucleotide variantAtrichia with papular lesions|Alopecia universalis congenita
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.