rs12967855

This variant is located in the CELF4 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 1.02
p 1.0e-19
N 807,553
Meta-analysisLarge GWAS
European
Allele A
OR 0.03
p 8.0e-16
N 1,820,689
Large GWAS
multi-ancestry
Allele A
OR 0.03
p 2.0e-18
N 1,349,887
Large GWAS
European
Allele A
OR 1.03
p 2.0e-9
N 332,622
Large GWAS
European

health trait

Allele A
OR 0.01
p 5.0e-15
N 405,979
Large GWAS
European

smoking behavior trait

Allele A
OR 0.01
p 3.0e-8
N 462,690
Large GWAS
European

household income

Allele G
OR 0.01
p 2.0e-9
N 286,301
Large GWAS
European

About CELF4

Members of the CELF/BRUNOL protein family contain two N-terminal RNA recognition motif (RRM) domains, one C-terminal RRM domain, and a divergent segment of 160-230 aa between the second and third RRM domains. Members of this protein family regulate pre-mRNA alternative splicing and may also be involved in mRNA editing, and translation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

View all CELF4 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…