Variant: rs11157436 

    present in Gene: TRAV30
    present in Chromosome: 14
    Position on Chromosome: 22168978
    Alleles of this Variant: C/T

rs11157436 in TRAV30 gene and ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO PMID 28447399 2017 Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study.

rs11157436 in TRAV30 gene and AIDS, PROGRESSION TO PMID 28447399 2017 Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study.

rs11157436 in TRAV30 gene and Adolescent idiopathic scoliosis PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.

rs11157436 in TRAV30 gene and HIV-1 infection PMID 28447399 2017 Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study.

rs11157436 in TRAV30 gene and HIV-1, RESISTANCE TO PMID 28447399 2017 Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study.

rs11157436 in TRAV30 gene and HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO PMID 28447399 2017 Genome-wide association study of HIV-associated neurocognitive disorder (HAND): A CHARTER group study.

rs11157436 in TRAV30 gene and SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 PMID 30019117 2018 The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.