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SNP information rs2234358

RS2234358

Normal allele: TT

The CXCR6 gene as a novel chemokine receptor involved in long-term prevention of AIDS progression.

Polymorphism rs2234358 is related to topics like this:

Genetic hiv

HIV, a virus that causes immunodeficiency in humans, belongs to the Lentivirus genus in the...

Research and publications:

  20704485   Multiple-cohort genetic association study reveals CXCR6 as a new chemokine receptor involved in long-term nonprogression to AIDS.

  21221856   The search for host genetic factors of HIV/AIDS pathogenesis in the post-genome era: progress to date and new avenues for discovery.

  22474614   Host genes important to HIV replication and evolution.

  22920050   Genome-wide association studies on HIV susceptibility, pathogenesis and pharmacogenomics.

  24240316   Host genomic HIV restriction factors modulate the response to dendritic cell-based treatment against HIV-1.

  24999842   Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus.

  27810495   Psoriasis risk SNPs and their association with HIV-1 control.

  28374494   Immunogenetic profiling of 23 SNPs of cytokine and chemokine receptor genes through a minisequencing technique: Design, development and validation.

  28428094   CXCR6 gene characterization in two ethnically distinct South African populations and association with viraemic disease control in HIV-1-infected black South African individuals.

  28456591   Polymorphisms of chemokine receptor genes and clearance of hepatitis C virus infection in Chinese population.

  35402715   Chemokine receptor CXCR6 gene polymorphism and treatment response of chronic hepatitis C virus in Egyptian patients.

Stroke genes

Ischemic stroke has a multifactorial etiology, with genetic causes playing a significant role,...

ADHD is it genetic

ADHD, a behavioral disorder that usually commences during childhood, is marked by a brief attention...

Epilepsy genes

If seizures are caused by a known or presumed genetic defect or issue related to epilepsy, it is...

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