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SNP information rs162036

RS162036

Normal allele: AA

Disorders of intracellular metabolism of cobalamin. Positive effect on the efficacy of folic acid therapy in patients with hyperhomocysteinaemia.

Polymorphism rs162036 is related to topics like this:

Folate and mthfr

MTHFR is an enzyme crucial for converting folic acid into an active form known as L-methylfolate,...

Mthfr and B12

Many individuals carry MTHFR mutations without being aware of their MTHFR status, while only a...

DNA methylation genes

The Genetic Methylation Check examines your DNA to offer insights into your unique methylation...

Mitochondria dna

The mitochondria contain circular chromosomes known as mitochondrial DNA and are organelles...

Hereditary gastric cancer

Gastric cancer is the third leading cause of cancer-related deaths worldwide, with a 5-year...

Research and publications:

  19064578   No association of single nucleotide polymorphisms in one-carbon metabolism genes with prostate cancer risk

  19112534   Lack of association of polymorphisms in homocysteine metabolism genes with pseudoexfoliation syndrome and glaucoma

  19493349   118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects

  19683694   Genetic association study of putative functional single nucleotide polymorphisms of genes in folate metabolism and spina bifida

  19936946   Germline polymorphisms in the one-carbon metabolism pathway and DNA methylation in colorectal cancer

  20445095   Colloquium paper: human adaptations to diet, subsistence, and ecoregion are due to subtle shifts in allele frequency.

  20718043   Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome

  21211571   MTHFR and MTRR genotype and haplotype analysis and colorectal cancer susceptibility in a case-control study from the Czech Republic.

  22496743   Genetic variant of AMD1 is associated with obesity in urban Indian children.

  23446900   One-carbon metabolism factors and leukocyte telomere length.

  23940529   Roles of genetic polymorphisms in the folate pathway in childhood acute lymphoblastic leukemia evaluated by Bayesian relevance and effect size analysis.

  24048206   Neural tube defects, folic acid and methylation.

  24524080   The effect of multiple single nucleotide polymorphisms in the folic acid pathway genes on homocysteine metabolism.

  25227144   Folate-related polymorphisms in gastrointestinal stromal tumours: susceptibility and correlation with tumour characteristics and clinical outcome.

  27404801   Joint effects of folate intake and one-carbon-metabolizing genetic polymorphisms on breast cancer risk: a case-control study in China.

  28253292   Polymorphisms associated with a tropical climate and root crop diet induce susceptibility to metabolic and cardiovascular diseases in Solomon Islands.

  29644956   Genetic polymorphisms of key enzymes in folate metabolism affect the efficacy of folate therapy in patients with hyperhomocysteinaemia.

  31377750   Targeted Next-Generation Sequencing Identifies Novel Sequence Variations of Genes Associated with Nonobstructive Azoospermia in the Han Population of Northeast China.

  32203239   Association of genetic and epigenetic variants in one-carbon metabolism gene with folate treatment response in hyperhomocysteinaemia.

  33195260   Non-syndromic Cleft Palate: An Overview on Human Genetic and Environmental Risk Factors.

  35434830   Analysis of the frequency distribution of five single-nucleotide polymorphisms of the MTRRgene in a Chinese pediatric population with acute lymphoblastic leukemia.

Mthfr and magnesium DNA

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Zinc finger protein

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Wilson disease gene

Wilson's disease is an autosomal recessive condition, necessitating that both parents carry at...

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