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SNP information rs9303277

RS9303277

Normal allele: CC

Polymorphism rs9303277 is related to topics like this:

Lupus is it genetic

It is now well understood that lupus is caused by both environmental and genetic factors. At...


Research and publications:

  19426955   Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene.

  19458352   Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants.

  19714205   Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children.

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

  20372189   A sequence variant on 17q21 is associated with age at onset and severity of asthma.

  20639880   Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis.

  20698975   Asthma-susceptibility variants identified using probands in case-control and family-based analyses.

  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.

  23154084   Examination of the relationship between variation at 17q21 and childhood wheeze phenotypes.

  23157251   Variants in the 17q21 asthma susceptibility locus are associated with allergic rhinitis in the Japanese population.

  23755072   Using eQTL weights to improve power for genome-wide association studies: a genetic study of childhood asthma.

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

  25690649   Multiple genetic variants associated with primary biliary cirrhosis in a Han Chinese population.

  26603569   ORMDL3 contributes to the risk of atherosclerosis in Chinese Han population and mediates oxidized low-density lipoprotein-induced autophagy in endothelial cells.

  28056976   A novel approach to genome-wide association analysis identifies genetic associations with primary biliary cholangitis and primary sclerosing cholangitis in Polish patients.

  28668238   Genetic variants and risk of asthma in an American Indian population.

  32977850   Epigenomics and transcriptomics of systemic sclerosis CD4+ T cells reveal long-range dysregulation of key inflammatory pathways mediated by disease-associated susceptibility loci.

  33963941   Association of Gasdermin B Gene GSDMB Polymorphisms with Risk of Allergic Diseases.

  34919286   17q12-21 risk-variants influence cord blood immune regulation and multitrigger-wheeze.

Crohn's disease genetic

A chronic disorder known as Crohn's disease is a multi-faceted condition that primarily impacts the...

Is rheumatoid arthritis genetic

Chronic abnormal inflammation is the hallmark of rheumatoid arthritis, a disease that primarily...

Hereditary pancreatitis

Pancreatitis is a multifaceted ailment that can stem from various sources. If pancreatitis arises...

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