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SNP information rs9368699

RS9368699

Normal allele: TT

A single nucleotide polymorphism that favours natural long-term slowing of HIV infection progression.

Polymorphism rs9368699 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:

  20876667   Genome-wide significant associations for variants with minor allele frequency of 5% or less--an overview: A HuGE review.

  21107268   Screening low-frequency SNPS from genome-wide association study reveals a new risk allele for progression to AIDS.

  21498636   Genome-wide "pleiotropy scan" identifies HNF1A region as a novel pancreatic cancer susceptibility locus.

  22238471   Single-nucleotide polymorphism-defined class I and class III major histocompatibility complex genetic subregions contribute to natural long-term nonprogression in HIV infection.

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

  23886662   A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis.

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

  28449694   The MHC locus and genetic susceptibility to autoimmune and infectious diseases.

  31137555   Long Noncoding RNA HCP5, a Hybrid HLA Class I Endogenous Retroviral Gene: Structure, Expression, and Disease Associations.

Stroke genes

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ADHD is it genetic

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Epilepsy genes

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

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