rs10453119 - TPD52
Magnitude 2.2 · 1 study on file
Reported associations
-
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
Auto-generated from study metadata. AI-synthesised commentary is added when this entry is regenerated through content-service's LLM mode.
Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Discuss with your doctor
-
TPD52 variant and rheumatoid arthritis genetic risk Moderate
Genetic variant in TPD52 is associated with increased rheumatoid arthritis risk; clinical discussion enables personalized screening and monitoring strategy
Schedule appointment to discuss RA genetic risk assessment and surveillance plan
Screening
-
Rheumatoid arthritis symptom monitoring Moderate
Genetic risk variant warrants heightened awareness for early signs of RA to enable timely clinical intervention
Report new joint pain, swelling, or morning stiffness lasting over 30 minutes to healthcare provider