rs10190052 - LINC01875 - TMEM18

Magnitude 2.2 · 1 study on file

Reported associations

  • Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility - Unknown journal (n.d.) · Unknown authors · PubMed 24509480

    ABSTRACT: To further understanding of the genetic basis of type 2 diabetes (T2D) susceptibility, we aggregated published meta-analyses of genome-wide association studies (GWAS) including 26,488 cases and 83,964 controls of European, East Asian, South Asian, and Mexican and Mexican American ancestry. We observed significant excess in directional consistency of T2D risk alleles across ancestry groups, even at SNPs demonstrating only weak evidence of association. By following up the strongest signals of association from the trans-ethnic meta-analysis in an additional 21,491 cases and 55,647 controls of European ancestry, we identified seven novel T2D susceptibility loci. Furthermore, we observed considerable improvements in fine-mapping resolution of common variant association signals at seve


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Lifestyle context

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

Discuss with your doctor

  • increased genetic diabetes risk Moderate

    rs10190052 C allele associated with 7 percent higher type 2 diabetes risk per allele in large genome-wide study

Screening

  • fasting glucose and HbA1c Moderate

    C allele carriers have increased type 2 diabetes genetic predisposition, warranting proactive glucose monitoring

    Discuss screening frequency with healthcare provider