rs10277680 - CUX1
Magnitude 2.2 · 1 study on file
Reported associations
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Global multi-ancestry genome-wide analyses identify genes and biological pathways associated with thyroid cancer and benign thyroid diseases - Unknown journal (n.d.) · Unknown authors · PubMed 41644669
ABSTRACT: Thyroid diseases are common and highly heritable. We performed a meta-analysis of genome-wide association studies from 19 biobanks for five thyroid diseases: thyroid cancer (ThC), benign nodular goiter, Graves' disease, lymphocytic thyroiditis and primary hypothyroidism. We analyzed genetic association data from ~2.9 million genomes and identified 313 known and 570 new independent loci linked to thyroid diseases. We discovered genetic correlations between ThC, benign nodular goiter and autoimmune thyroid diseases (rg = 0.16-0.97). Telomere maintenance genes contributed to benign and malignant thyroid nodular disease risk, whereas cell cycle, DNA repair and damage response genes were associated with ThC. We propose a paradigm that explains genetic predisposition to benign
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Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Discuss with your doctor
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thyroid health monitoring given genetic predisposition Moderate
GWAS association indicates increased hypothyroidism risk warranting personalized screening strategy
Discuss optimal screening frequency and symptom awareness with healthcare provider
Screening
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thyroid function testing (TSH, free T4) Moderate
rs10277680 risk allele A is associated with increased hypothyroidism risk in large GWAS
Annual screening if asymptomatic; more frequent monitoring if fatigue, weight gain, or cold intolerance develops