rs79172804

This is a intron variant variant in the LINC02210-CRHR1 gene.

GWAS Catalog Trait Associations (5)

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

neuroimaging measurement

Allele A
OR 0.14
p 3.0e-27
N 20,859
Major Consortium StudyLarge GWAS
European

serum albumin amount

Zoodsma M et al. A genetic map of human metabolism across the allele frequency spectrum. Nature Genetics 57(10):2445-2455 (2025)
Allele A
OR 0.03
p 4.0e-25
N 450,015
Large GWAS
multi-ancestry

post-traumatic stress disorder symptom measurement

Allele A
OR 0.44
p 2.0e-13
N 237,725
Major Consortium StudyLarge GWAS
multi-ancestry

amount of iron in brain

Allele G
OR 0.05
p 5.0e-9
N 39,533
Major Consortium StudyLarge GWAS
European

white matter integrity

Allele A
OR 0.09
p 1.0e-11
N 20,860
Major Consortium StudyLarge GWAS
European

About LINC02210-CRHR1

This locus represents naturally occurring readthrough transcription between neighboring genes CRHR1-IT1, CRHR1 intronic transcript 1 (Gene ID: 147081) and CRHR1, corticotropin releasing hormone receptor 1 (Gene ID: 1394) on chromosome 17. The readthrough transcript encodes a protein that shares sequence identity with the product of the CRHR1 gene. [provided by RefSeq, Dec 2016]

View all LINC02210-CRHR1 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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