rs10200279 - FLACC1, CASP8
Magnitude 2.2 · 3 studies on file
Reported associations
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Genome-wide meta-analysis identifies eight new susceptibility loci for cutaneous squamous cell carcinoma - Unknown journal (n.d.) · Unknown authors · PubMed 32041948
ABSTRACT: Cutaneous squamous cell carcinoma (SCC) is one of the most common cancers in the United States. Previous genome-wide association studies (GWAS) have identified 14 single nucleotide polymorphisms (SNPs) associated with cutaneous SCC. Here, we report the largest cutaneous SCC meta-analysis to date, representing six international cohorts and totaling 19,149 SCC cases and 680,049 controls. We discover eight novel loci associated with SCC, confirm all previously associated loci, and perform fine mapping of causal variants. The novel SNPs occur within skin-specific regulatory elements and implicate loci involved in cancer development, immune regulation, and keratinocyte differentiation in SCC susceptibility. The authors perform a meta-analysis of cutaneous squamous cell carcinoma, iden
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Genome-wide association meta-analyses combining multiple risk phenotypes provides insights into the genetic architecture of cutaneous melanoma susceptibility - Unknown journal (n.d.) · Unknown authors · PubMed 32341527
ABSTRACT: Most genetic susceptibility to cutaneous melanoma remains to be discovered. Meta-analysis genome-wide association study (GWAS) of 36,760 melanoma cases (67% newly-genotyped) and 375,188 controls identified 54 significant loci with 68 independent SNPs. Analysis of risk estimates across geographical regions and host factors suggests the acral melanoma subtype is uniquely unrelated to pigmentation. Combining this meta-analysis with nevus count and hair color GWAS, and transcriptome association approaches, uncovered 31 potential secondary loci, for a total of 85 cutaneous melanoma susceptibility loci. These findings provide substantial insights into cutaneous melanoma genetic architecture, reinforcing the importance of nevogenesis, pigmentation, and telomere maintenance together with
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Genome-Wide Association Study Identifies Genetic Associations with Perceived Age - Unknown journal (n.d.) · Unknown authors · PubMed 32339537
ABSTRACT: Failure of dermal protection or repair mechanisms might lead to visibly aged skin. The study aimed to identify genetic associations with perceived age. A genome-wide association study was undertaken in 423,992 adult participants of UK Biobank, using questionnaire data on perceived age and genetic data imputed to the Haplotype Reference Consortium imputation panel. The study identified 74 independently associated genetic loci, to our knowledge previously unreported (P < 5 × 10−8), which were enriched for cell signaling pathways, including the NEK6 and SMAD2 subnetworks. Common genetic variation was estimated to account for 14% of variation in perceived age, and the heritability of perceived age was partially shared with that of 75 other traits, including multiple traits repres
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Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Screening
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dermatological skin cancer screening Moderate
T allele impairs CASP8-mediated apoptosis, allowing UV-damaged cells to escape elimination and increasing risk of squamous and basal cell carcinomas.
Discuss with dermatologist about baseline examination and follow-up interval; consider every 1-2 years.