rs11209947 - LINC02796
Magnitude 2.2 · 1 study on file
Reported associations
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Genetic architecture of human thinness compared to severe obesity - Unknown journal (n.d.) · Unknown authors · PubMed 30677029
ABSTRACT: The variation in weight within a shared environment is largely attributable to genetic factors. Whilst many genes/loci confer susceptibility to obesity, little is known about the genetic architecture of healthy thinness. Here, we characterise the heritability of thinness which we found was comparable to that of severe obesity (h2 = 28.07 vs 32.33% respectively), although with incomplete genetic overlap (r = -0.49, 95% CI [-0.17, -0.82], p = 0.003). In a genome-wide association analysis of thinness (n = 1,471) vs severe obesity (n = 1,456), we identified 10 loci previously associated with obesity, and demonstrate enrichment for established BMI-associated loci (pbinomial = 3.05x10-5). Simulation analyses showed that different association results between the extremes were likely in
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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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Personalized obesity prevention and lifestyle plan High
Genetic predisposition through NEGR1 pathways suggests value of proactive, individualized prevention strategy
Schedule visit to review family history, current diet, activity level, and establish baseline metrics for tracking
Screening
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Obesity and metabolic risk monitoring High
rs11209947-A is associated with 1.17-fold increased severe obesity risk through NEGR1-mediated energy homeostasis
Annual screening: BMI, waist circumference, fasting glucose, lipid panel, liver function tests