rs114156513 - NBPF18P - S100A11
Magnitude 2.2 · 1 study on file
Reported associations
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Genome-Wide Integration of Genetic and Genomic Studies of Atopic Dermatitis: Insights into Genetic Architecture and Pathogenesis. - The Journal of investigative dermatology (2022) · Chen Y, Chen W · PubMed 35577104
Atopic dermatitis (AD) is a common heterogeneous, chronic, itching, and inflammatory skin disease. Genetic studies have identified multiple AD susceptibility genes. However, the genetic architecture of AD has not been elucidated. In this study, we conducted a large-scale meta-analysis of AD (35,647 cases and 1,013,885 controls) to characterize the genetic basis of AD. The heritability of AD in different datasets varied from 0.6 to 7.1%. We identified 31 previously unreported genes by integrating multiomics data. Among the 31 genes, MCL1 was identified as a potential treatment target for AD by mediating gene‒drug interactions. Tissue enrichment analyses and phenome-wide association study provided strong support for the role of the hemic and immune systems in AD. Across 1,207 complex trait
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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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discuss genetic atopic dermatitis risk and prevention Moderate
genetic predisposition identified via large-scale GWAS; early discussion enables proactive management
Lifestyle
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fragrance-free moisturizer application Moderate
maintains skin barrier integrity, reducing transepidermal water loss and irritant penetration in AD-prone skin
apply within 3 minutes of bathing, at least twice daily
Screening
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screen for atopic dermatitis symptoms Moderate
SNP rs114156513 (risk allele T) confers significantly increased genetic risk for atopic dermatitis
periodic dermatological assessment, especially following skin irritation or stress