rs11927381 - IGF2BP2

Magnitude 2.2 · 5 studies on file

Reported associations

  • Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium - Unknown journal (n.d.) · Unknown authors · PubMed 35399580

    ABSTRACT: Hispanic/Latinos have been underrepresented in genome-wide association studies (GWAS) for anthropometric traits despite their notable anthropometric variability, ancestry proportions, and high burden of growth stunting and overweight/obesity. To address this knowledge gap, we analyzed densely imputed genetic data in a sample of Hispanic/Latino adults to identify and fine-map genetic variants associated with body mass index (BMI), height, and BMI-adjusted waist-to-hip ratio (WHRadjBMI). We conducted a GWAS of 18 studies/consortia as part of the Hispanic/Latino Anthropometry (HISLA) Consortium (stage 1, n = 59,771) and generalized our findings in 9 additional studies (stage 2, n = 10,538). We conducted a trans-ancestral GWAS with summary statistics from HISLA stage 1 and existing

  • Diversity and scale: Genetic architecture of 2068 traits in the VA Million Veteran Program - Unknown journal (n.d.) · Unknown authors · PubMed 39024449

    ABSTRACT: INTRODUCTION: Findings from genome-wide association studies (GWASs) have provided foundational knowledge of the genetic basis of disease, facilitating precision approaches for prevention and treatment. Current GWAS results are limited by underrepresentation of individuals from diverse populations, leading to concerns with generalizability regarding our knowledge of the relationships between genes, traits, and disease. The Department of Veterans Affairs (VA) Million Veteran Program (MVP), one of the largest US-based biobanks, addresses this need; 29% of MVP comprises individuals genetically similar to African (AFR), Admixed American (AMR), and East Asian (EAS) reference populations. With over 635,000 participants and more than 44.3M genotyped variants linked with detailed phenotyp

  • Multi-ethnic genome-wide association study identifies novel locus for type 2 diabetes susceptibility - Unknown journal (n.d.) · Unknown authors · PubMed 27189021

    ABSTRACT: Genome-wide association studies (GWAS) have traditionally been undertaken in homogeneous populations from the same ancestry group. However, with the increasing availability of GWAS in large-scale multi-ethnic cohorts, we have evaluated a framework for detecting association of genetic variants with complex traits, allowing for population structure, and developed a powerful test of heterogeneity in allelic effects between ancestry groups. We have applied the methodology to identify and characterise loci associated with susceptibility to type 2 diabetes (T2D) using GWAS data from the Resource for Genetic Epidemiology on Adult Health and Aging, a large multi-ethnic population-based cohort, created for investigating the genetic and environmental basis of age-related diseases. We ident

  • Pan-cancer and cross-population genome-wide association studies dissect shared genetic backgrounds underlying carcinogenesis - Unknown journal (n.d.) · Unknown authors · PubMed 37340002

    ABSTRACT: Integrating genomic data of multiple cancers allows de novo cancer grouping and elucidating the shared genetic basis across cancers. Here, we conduct the pan-cancer and cross-population genome-wide association study (GWAS) meta-analysis and replication studies on 13 cancers including 250,015 East Asians (Biobank Japan) and 377,441 Europeans (UK Biobank). We identify ten cancer risk variants including five pleiotropic associations (e.g., rs2076295 at DSP on 6p24 associated with lung cancer and rs2525548 at TRIM4 on 7q22 nominally associated with six cancers). Quantifying shared heritability among the cancers detects positive genetic correlations between breast and prostate cancer across populations. Common genetic components increase the statistical power, and the large-scale meta

  • Trans-Ethnic Analysis of Metabochip Data Identifies Two New Loci Associated with BMI - Unknown journal (n.d.) · Unknown authors · PubMed 29381148

    ABSTRACT: Objective Body mass index (BMI) is commonly used to assess obesity, which is associated with numerous diseases and negative health outcomes. BMI has been shown to be a heritable, polygenic trait, with close to 100 loci previously identified and replicated in multiple populations. We aim to replicate known BMI loci and identify novel associations in a trans-ethnic study population. Subjects Using eligible participants from the Population Architecture using Genomics and Epidemiology (PAGE) consortium, we conducted a trans-ethnic meta-analysis of 102,514 African Americans, Hispanics, Asian/Native Hawaiian, Native Americans and European Americans. Participants were genotyped on over 200,000 SNPs on the Illumina Metabochip custom array, or imputed into the 1000 Genomes Project (Phase


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Lifestyle context

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

Diet

  • Refined carbohydrates and added sugars High

    IGF2BP2 rs11927381 C-allele increases T2D risk; limiting refined carbohydrates reduces metabolic stress and progression

    Minimize sugary beverages, white bread, pastries; choose whole grains and legumes

Discuss with your doctor

  • Personalized T2D prevention plan based on genetic risk High

    rs11927381 C-allele substantially elevates T2D risk; physicians can optimize screening intervals and interventions

    Share genotype; discuss screening frequency, lifestyle support, and pharmacotherapy eligibility

Exercise

  • Regular cardiovascular and resistance exercise program High

    IGF2BP2 rs11927381 C-allele carriers have increased T2D susceptibility; exercise is the most effective prevention strategy

    Minimum 150 minutes per week moderate-intensity aerobic activity; add 2-3 resistance sessions weekly

Screening

  • Annual fasting glucose and hemoglobin A1c testing High

    IGF2BP2 rs11927381 C-allele confers 14% increased T2D risk per allele; early detection enables intervention

    Baseline fasting glucose and HbA1c; repeat annually or per physician guidance