rs3769821
This variant is located in the CASP8 gene.
▶GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
GWAS Catalog Trait Associations (2)
Genome-wide significant associations (p < 5×10⁻⁸) from the NHGRI-EBI GWAS Catalog.
breast carcinoma
non-small cell lung carcinoma
▶Research that mentions this SNP (1)
▶Polymorphisms in the promoter region of the CASP8 gene are not associated with non-Hodgkin’s lymphoma in Chinese patientsAssociationN=379Mei-Sheng Xiao et al.(2011)· Annals of Hematology
This case-control study investigated three CASP8 gene promoter polymorphisms (rs3834129, rs3769821, and rs113686495) in relation to non-Hodgkin's lymphoma (NHL) in Chinese patients across two cohorts (Kunming n=64 cases/133 controls; Shanghai n=75 cases/107 controls). Found no statistically significant association between any of the three variants and NHL risk, and luciferase assays showed no functional difference in promoter activity between variant alleles, contradicting previous reports from other populations.
About CASP8
This gene encodes a member of the cysteine-aspartic acid protease (caspase) family. Sequential activation of caspases plays a central role in the execution-phase of cell apoptosis. Caspases exist as inactive proenzymes composed of a prodomain, a large protease subunit, and a small protease subunit. Activation of caspases requires proteolytic processing at conserved internal aspartic residues to generate a heterodimeric enzyme consisting of the large and small subunits. This protein is involved in the programmed cell death induced by Fas and various apoptotic stimuli. The N-terminal FADD-like death effector domain of this protein suggests that it may interact with Fas-interacting protein FADD. This protein was detected in the insoluble fraction of the affected brain region from Huntington disease patients but not in those from normal controls, which implicated the role in neurodegenerative diseases. Many alternatively spliced transcript variants encoding different isoforms have been described, although not all variants have had their full-length sequences determined. [provided by RefSeq, Jul 2008]
View all CASP8 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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