Gene entry
HCRTR2
hypocretin receptor 2
- Chromosome
- 6
- Cytoband
- 6p12.1
- Variants (rsID)
- 38
HCRTR2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p12.1). Its official name is “hypocretin receptor 2”. The reference table lists 38 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs2653349Not classifiedmissense_variantCluster Headache|Headache|Alzheimer Disease|Goiter|Schizotypal Personality Disorder|Mental Depression|Major Depressive Disorder|Smoking As a Quantitative Trait Locus 3|Tobacco Addiction|Depression|Sleep Disorder|Mood Disorder|Narcolepsy|Hypersomnia
Other listed variants
- rs3122169
- rs3134705
- rs4434473
- rs4712099
- rs6927478
- rs6937878
- rs7766546
- rs7768760
- rs7773759
- rs9349764
- rs9357851
- rs9367616
- rs9367618
- rs9370389
- rs9370399
- rs9382460
- rs10456181
- rs12111375
- rs12209331
- rs12209538
- rs12525431
- rs13196636
- rs13200042
- rs17682926
- rs17750259
- rs41271312
- rs57819349
- rs72977410
- rs72978538
- rs79287400
- rs112934230
- rs115829335
- rs117957186
- rs140040663
- rs140883768
- rs141299250
- rs151196968
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.