rs11777380 - CCN4
Magnitude 2.2 · 1 study on file
Reported associations
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Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis - Unknown journal (n.d.) · Unknown authors · PubMed 36333501
ABSTRACT: Rheumatoid arthritis (RA) is a highly heritable complex disease with unknown etiology. Multi-ancestry genetic research of RA promises to improve power to detect genetic signals, fine-mapping resolution and performances of polygenic risk scores (PRS). Here, we present a large-scale genome-wide association study (GWAS) of RA, which includes 276,020 samples from five ancestral groups. We conducted a multi-ancestry meta-analysis and identified 124 loci (P < 5 × 10−8), of which 34 are novel. Candidate genes at the novel loci suggest essential roles of the immune system (for example, TNIP2 and TNFRSF11A) and joint tissues (for example, WISP1) in RA etiology. Multi-ancestry fine-mapping identified putatively causal variants with biological insights (for example, LEF1). Moreover, PRS
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Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
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Genetic predisposition to seropositive RA Moderate
CCN4 variant associated with seropositive rheumatoid arthritis risk
Review RA risk, baseline screening options, and monitoring strategy