rs12552

This is a 3 prime utr variant variant in the OLFM4 gene.

GWAS Catalog Trait Associations (6)

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

major depressive disorder

Allele A
OR 1.04
p 6.0e-19
N 480,359
Large GWAS
European
Allele A
OR 6.37
p 2.0e-10
N 688,809
Meta-analysisLarge GWAS
European
Allele A
OR 0.04
p 8.0e-9
N 326,113
Large GWAS
European

intelligence

Allele A
OR 0.02
p 3.0e-8
N 248,482
Large GWAS
European

autism spectrum disorder, major depressive disorder

Allele A
OR 0.05
p 4.0e-8
N 470,365
Large GWAS
European

insomnia

Allele A
OR 0.01
p 1.0e-19
N 1,216,033
Meta-analysisLarge GWAS
European

About OLFM4

This gene was originally cloned from human myeloblasts and found to be selectively expressed in inflammed colonic epithelium. This gene encodes a member of the olfactomedin family. The encoded protein is an antiapoptotic factor that promotes tumor growth and is an extracellular matrix glycoprotein that facilitates cell adhesion. [provided by RefSeq, Mar 2011]

View all OLFM4 variants →

Gene information from NCBI Gene. Variant classifications from ClinVar.

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