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SNP information rs567754

Normal allele: CC

The detected C/T genotype contains a risky "T" allele, which potentially reduces the efficiency of the methylation process and may impair health outcomes.

Polymorphism rs567754 is related to topics like this:

Methylation and homocysteine


Research and publications:

  18457970   Human betaine-homocysteine methyltransferase (BHMT) and BHMT2: common gene sequence variation and functional characterization.

  19048631   Oral facial clefts and gene polymorphisms in metabolism of folate/one-carbon and vitamin A: a pathway-wide association study

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

  21093336   Betaine-homocysteine methyltransferase: human liver genotype-phenotype correlation.

  21146954   Genes and abdominal aortic aneurysm

  21254359   Folate pathway and nonsyndromic cleft lip and palate.

  23205182   A genome-wide association study of variations in maternal cardiometabolic genes and risk of placental abruption.

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

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