rs10162002 - LINC00327

Magnitude 2.8 · 1 study on file

Reported associations

  • Novel Associations for Hypothyroidism Include Known Autoimmune Risk Loci - Unknown journal (n.d.) · Unknown authors · PubMed 22493691

    ABSTRACT: Hypothyroidism is the most common thyroid disorder, affecting about 5% of the general population. Here we present the current largest genome-wide association study of hypothyroidism, in 3,736 cases and 35,546 controls. Hypothyroidism was assessed via web-based questionnaires. We identify five genome-wide significant associations, three of which are well known to be involved in a large spectrum of autoimmune diseases: rs6679677 near PTPN22, rs3184504 in SH2B3, and rs2517532 in the HLA class I region (-values , , and , respectively). We also report associations with rs4915077 near VAV3 (-value ) and rs925489 near FOXE1 (-value ). VAV3 is involved in immune function, and FOXE1 and PTPN22 have previously been associated with hypothyroidism. Although the HLA class I region and SH2B3 h


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Lifestyle context

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

Discuss with your doctor

  • genetic risk for hypothyroidism Moderate

    GWAS studies show rs10162002 A allele confers increased hypothyroidism risk; clinical context helps guide monitoring strategy

Screening

  • thyroid function screening (TSH, free T4) Moderate

    rs10162002 A allele increases hypothyroidism risk; baseline thyroid assessment enables early detection

    baseline TSH and free T4; consider periodic monitoring