rs10810650 - BNC2 - RN7SL720P

Magnitude 2.2 · 3 studies on file

Reported associations

  • 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

  • Genome-wide association studies in a large Korean cohort identify quantitative trait loci for 36 traits and illuminate their genetic architectures - Unknown journal (n.d.) · Unknown authors · PubMed 40436827

    ABSTRACT: Genome-wide association studies (GWAS) have predominantly focused on European ancestry populations, limiting biological discoveries across diverse populations. Here we report GWAS findings from 153,950 individuals across 36 quantitative traits in the Korean Cancer Prevention Study-II (KCPS2) Biobank. We discovered 301 previously unreported genetic loci in KCPS2, including an association between thyroid-stimulating hormone and CD36. Meta-analysis with the Korean Genome and Epidemiology Study, Biobank Japan, Taiwan Biobank, and UK Biobank identified 4588 loci that were not significant in any contributing GWAS. We describe differences in genetic architectures across these East Asian and European samples. We also highlight East Asian specific associations, including a known pleiotrop

  • Genome-wide association study in 176,678 Europeans reveals genetic loci for tanning response to sun exposure - Unknown journal (n.d.) · Unknown authors · PubMed 29739929

    ABSTRACT: The skin's tendency to sunburn rather than tan is a major risk factor for skin cancer. Here we report a large genome-wide association study of ease of skin tanning in 176,678 subjects of European ancestry. We identify significant association with tanning ability at 20 loci. We confirm previously identified associations at six of these loci, and report 14 novel loci, of which ten have never been associated with pigmentation-related phenotypes. Our results also suggest that variants at the AHR/AGR3 locus, previously associated with cutaneous malignant melanoma the underlying mechanism of which is poorly understood, might act on disease risk through modulation of tanning ability. The skin's tanning response to sun exposure shows great interindividual variability. Here, Visconti


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Lifestyle context

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

Discuss with your doctor

  • Melanoma risk stratification and surveillance plan High

    rs10810650 C allele shows genome-wide significant association with increased melanoma risk and reduced protective tanning response

Lifestyle

  • Avoid peak sun hours and wear protective clothing High

    Reduced melanin production from rs10810650 C allele combined with elevated melanoma risk requires comprehensive UV avoidance strategy

    Limit sun exposure 10am-4pm, wear wide-brimmed hat and UV-blocking clothing

  • Daily broad-spectrum SPF 30+ sunscreen High

    rs10810650 C allele reduces tanning response and increases melanoma risk, indicating fair skin phenotype requiring enhanced UV protection

    Apply SPF 30+ daily, reapply every 2 hours during sun exposure

Screening

  • Annual full-body skin examination by dermatologist High

    rs10810650 C allele confers significantly increased melanoma susceptibility (p=9.00e-33, n=434,871)

    Schedule annual or semi-annual comprehensive skin examination