rs79986767

This is a intergenic variant variant in the HCRTR2 gene.

GWAS Catalog Trait Associations (6)

Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.

serum creatinine amount

Allele T
OR 0.07
p 3.0e-85
N 928,679
Large GWAS
multi-ancestry
Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele T
OR 0.09
p 7.0e-12
N 600,139
Major Consortium StudyLarge GWAS
multi-ancestry

hematocrit

Allele T
OR 0.05
p 7.0e-32
N 928,679
Large GWAS
multi-ancestry

blood urea nitrogen amount

Verma A et al. Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program. Science (new York, N.y.) 385(6706):eadj1182 (2024)
Allele T
OR 0.09
p 2.0e-11
N 599,920
Major Consortium StudyLarge GWAS
multi-ancestry

urolithiasis

Sakaue S et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics 53(10):1415-1424 (2021)
Allele C
OR 0.14
p 2.0e-8
N 667,072
Large GWAS
multi-ancestry

About HCRTR2

The protein encoded by this gene is a G-protein coupled receptor involved in the regulation of feeding behavior. The encoded protein binds the hypothalamic neuropeptides orexin A and orexin B. A related gene (HCRTR1) encodes a G-protein coupled receptor that selectively binds orexin A. [provided by RefSeq, Jan 2009]

View all HCRTR2 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

Community Wiki

No community notes yet for this variant. Sign in to start one.

Comments

Sign in to join the discussion.

Loading comments…