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SNP information rs4684847

RS4684847

Normal allele: CC

Polymorphism rs4684847 is related to topics like this:

Genetics and high blood pressure

Abnormally high blood pressure in the arteries, which transport blood from the heart to the rest of...

Research and publications:

  18263601   Single nucleotide polymorphisms in inflammation-related genes and mortality in a community-based cohort in Washington County, Maryland.

  18288282   Genetic polymorphisms of peroxisome proliferator-activated receptors and the risk of cardiovascular morbidity and mortality in a community-based cohort in washington county, Maryland

  19818126   Single nucleotide polymorphisms in obesity-related genes and all-cause and cause-specific mortality: a prospective cohort study

  23545576   Association of peroxisome proliferator-activated receptor α/δ/γ with obesity, and gene-gene interaction, in the Chinese Han population.

  24599720   Effect of obesity on the association between common variations in the PPAR gene and C-reactive protein level in Chinese Han population.

  24880474   Analysis on the association between PPARα/γ polymorphisms and lipoprotein(a) in a Chinese Han population.

  25987964   Role of peroxisome proliferator-activated receptors gene polymorphisms in type 2 diabetes and metabolic syndrome.

  26930606   Computational Characterization of Osteoporosis Associated SNPs and Genes Identified by Genome-Wide Association Studies.

  28123453   Interaction between peroxisome proliferator-activated receptor gamma polymorphism and obesity on type 2 diabetes in a Chinese Han population.

  29496354   Expression of the gene encoding PGC-1β in peripheral blood leukocytes and related gene variants in patients with Parkinson's disease.

  29652634   Emerging applications of genome-editing technology to examine functionality of GWAS-associated variants for complex traits.

  30181995   Haplotype Analysis of PPARγ Gene Polymorphisms and the Lipoprotein (a) Level.

  32190036   Association of Peroxisome Proliferator-Activated Receptors (PPARs) with Diabetic Retinopathy in Human and Animal Models: Analysis of the Literature and Genome Browsers.

  34502231   Common Genetic Aberrations Associated with Metabolic Interferences in Human Type-2 Diabetes and Acute Myeloid Leukemia: A Bioinformatics Approach.

  35124268   Mendelian Randomization Analysis Reveals No Causal Relationship Between Nonalcoholic Fatty Liver Disease and Severe COVID-19.

G20210A prothrombin mutation

The Prothrombin G20210A mutation, also known as Factor II mutation, is a hereditary trait that...

Schizophrenia is it genetic

A psychosis known as schizophrenia impacts an individual's thinking, sense of self, and...

Hereditary polyneuropathy

The peripheral nervous system is affected by a diverse range of diseases known as hereditary...

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