rs116784579 - NR2F2-AS1

Magnitude 2.2 · 1 study on file

Reported associations

  • Genome-wide analyses using UK Biobank data provide insights into the genetic architecture of osteoarthritis - Unknown journal (n.d.) · Unknown authors · PubMed 29559693

    ABSTRACT: Osteoarthritis is a common complex disease with huge public health burden. Here we perform a genome-wide association study for osteoarthritis using data across 16.5 million variants from the UK Biobank resource. Following replication and meta-analysis in up to 30,727 cases and 297,191 controls, we report 9 new osteoarthritis loci, in all of which the most likely causal variant is non-coding. For three loci, we detect association with biologically-relevant radiographic endophenotypes, and in five signals we identify genes that are differentially expressed in degraded compared to intact articular cartilage from osteoarthritis patients. We establish causal effects for higher body mass index, but not for triglyceride levels or genetic predisposition to type 2 diabetes, on osteoarthri


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Lifestyle context

Concrete actions anchored to the cited research. We do not prescribe, we describe.

Lifestyle

  • Weight maintenance and regular joint-protective activity Moderate

    rs116784579 C allele associates with 1.15x increased osteoarthritis risk; weight and activity modifications reduce joint loading

    Maintain BMI 18.5-24.9; perform 150 min/week moderate activity including resistance training

Screening

  • Joint symptoms screening Moderate

    C allele carriers have increased osteoarthritis susceptibility; early identification enables timely intervention

    Annual assessment for joint pain, swelling, or restricted mobility