rs20575

This is a protein-altering variant in the TNFRSF10A gene.

Research that mentions this SNP (2)

Evaluation of trail receptor 1 (DR4) polymorphisms C626G and A683C as risk factors of hepatocellular carcinoma
AssociationN=160Naglaa F. Alsalawy et al.(2018)· Journal of Medical Virology

This case-control study of 160 Egyptian patients with HCV-related liver disease evaluated two TRAIL receptor 1 (DR4) polymorphisms as risk factors for hepatocellular carcinoma (HCC). The C626G variant (rs20575) showed a significant association with HCC risk (OR=2.01 for C allele carriers, p=0.003), while A683C (rs20576) alone did not. The combined haplotype of C allele at rs20575 and A allele at rs20576 showed substantially increased HCC risk (OR=2.85, p>0.001).

Traits studied:HCCHepatocellular carcinoma
Associations between interleukin‐6 gene −174 C/G and −572 C/G polymorphisms and the risk of gastric cancer: A meta‐analysis
AssociationN=213Yan‐Wei Yin et al.(2012)· Journal of Surgical Oncology

Turkish case-control study examining TRAIL and TRAIL-DR4 gene polymorphisms in gastric cancer. Compared TRAIL C1595T (rs1131580) and TRAIL-DR4 C626G (rs20575) genotype frequencies between 50 gastric cancer patients and 163 healthy controls. No significant association found between either polymorphism and gastric cancer risk (p>0.256, p>0.189) or clinical parameters including tumor stage, lymph node involvement, distant metastasis, and perineural invasion. Serum TRAIL levels were also not significantly different between groups (p>0.33).

Traits studied:Gastric cancerGastric cancer susceptibility

About TNFRSF10A

The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is activated by tumor necrosis factor-related apoptosis inducing ligand (TNFSF10/TRAIL), and thus transduces cell death signal and induces cell apoptosis. Studies with FADD-deficient mice suggested that FADD, a death domain containing adaptor protein, is required for the apoptosis mediated by this protein. [provided by RefSeq, Jul 2008]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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