rs2352974

This is a downstream gene variant variant in the TRAIP gene.

GWAS Catalog Trait Associations (4)

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

intelligence

Allele C
OR 0.03
p 2.0e-31
N 254,641
Large GWAS
European
Allele C
OR 11.21
p 4.0e-29
N 269,867
Meta-analysisLarge GWAS
European

waist-hip ratio

Allele T
OR 0.02
p 6.0e-18
N 316,772
Meta-analysisLarge GWAS
European

Research that mentions this SNP (1)

Genome‐wide significant locus for Research Diagnostic Criteria Schizoaffective Disorder Bipolar type
Meta-analysisN=9,917Elaine K. Green et al.(2017)· American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

This meta-analysis of Research Diagnostic Criteria Schizoaffective Disorder Bipolar type (RDC-SABP) identified a genome-wide significant locus at rs2352974 in the TRAIP gene on chromosome 3p21.31 (P=4.37×10⁻⁸, OR=0.67). By combining WTCCC data (n=279 cases, n=2,938 controls) with an independent ImmunoChip replication sample (n=144 cases, n=6,559 controls), the study analyzed 10 SNPs previously associated with RDC-SABP. The TRAIP locus was not genome-wide significant in larger bipolar disorder or schizophrenia consortia datasets, suggesting it may represent a relatively specific genetic risk factor for the bipolar subtype of schizoaffective disorder.

Traits studied:RDC-SABPSchizoaffective Disorder Bipolar type

About TRAIP

This gene encodes a protein that contains an N-terminal RING finger motif and a putative coiled-coil domain. A similar murine protein interacts with TNFR-associated factor 1 (TRAF1), TNFR-associated factor 2 (TRAF2), and cylindromatosis. The interaction with TRAF2 inhibits TRAF2-mediated nuclear factor kappa-B, subunit 1 activation that is required for cell activation and protection against apoptosis. [provided by RefSeq, Jul 2008]

View all TRAIP 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…