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SNP information rs12603332

RS12603332

Normal allele: TT

Polymorphism rs12603332 is related to topics like this:

Is asthma hereditary

Asthma is a respiratory condition that involves inflammation of the airways and recurring episodes...

Research and publications:

  18310477   ORMDL3 gene is associated with asthma in three ethnically diverse populations.

  19732864   Allele-specific chromatin remodeling in the ZPBP2/GSDMB/ORMDL3 locus associated with the risk of asthma and autoimmune disease.

  21843571   Relationship between the 17q21 locus and adult asthma in a Czech population.

  21985515   Association of genetic variants in chromosome 17q21 and adult-onset asthma in a Chinese Han population.

  22271045   Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell lines.

  22370936   Genetic variants on 17q21 are associated with asthma in a Han Chinese population.

  24649901   Genetic variants of 17q21 are associated with childhood-onset asthma and related phenotypes in a northeastern Han Chinese population: a case-control study.

  25256354   Risk of childhood asthma is associated with CpG-site polymorphisms, regional DNA methylation and mRNA levels at the GSDMB/ORMDL3 locus.

  25729625   The Association of GSDMB and ORMDL3 Gene Polymorphisms With Asthma: A Meta-Analysis.

  28055272   rs12603332 is associated with male asthma patients specifically in urban areas of Lahore, Pakistan.

  28740106   Environment Changes Genetic Effects on Respiratory Conditions and Allergic Phenotypes.

  30644696   Investigating the Association of Orosomucoid 1-like 3 (ORMDL3) Gene Polymorphism (rs12603332) with Susceptibility to Allergic Asthma in Iranian Northwestern Azeri Population.

  31357023   Genetic variants in 17q12-21 locus and childhood asthma in Brazil: Interaction with Varicella zoster virus seropositivity.

  31929190   Decreased sphingolipid synthesis in children with 17q21 asthma-risk genotypes.

  32500120   CRISPRi-mediated functional analysis of lung disease-associated loci at non-coding regions.

  34525218   Single-base editing of rs12603332 on chromosome 17q21 with a cytosine base editor regulates ORMDL3 and ATF6α expression.

  34982638   Association between 17q21 variants and asthma predisposition in Pashtun population from Pakistan.

Infertility genetic

Approximately 15% of couples of reproductive age are affected by infertility, which is a complex...

Genetic hiv

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

Stroke genes

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

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