F2F5 APOE MTHFR

SNP Prevalence and Clinical References

This page provides prevalence data for the individual SNPs among different ethnicities along with clinical references that show the risk associations. 

Rs1801131
Folic acid, methylation and neural tube closure in humans
How Dietary Factors Affect DNA Methylation: Lesson from Epidemiological Studies
rs1801133
Increased breast cancer risk at high plasma folate concentrations among women with the MT HFR 677T allele
How Dietary Factors Affect DNA Methylation: Lesson from Epidemiological Studies
rs2187668
Multiple common variants for celiac disease influencing immune gene expression
The Gluten-Free Diet for Celiac Disease and Beyond
rs7454108
Effective Detection of Human Leukocyte Antigen Risk Alleles in Celiac Disease Using Tag Single Nucleotide Polymorphisms
The Gluten-Free Diet for Celiac Disease and Beyond
rs429358
Apolipoprotein E genotype, lifestyle and coronary artery disease: Gene-environment interaction analyses in the UK Biobank population
Apolipoprotein E genotype, lifestyle and coronary artery disease: Gene-environment interaction analyses in the UK Biobank population
Coagulation factor V gene 1691G>A polymorphism as an indicator for risk and prognosis of lower extremity deep venous thrombosis in Chinese Han population
Prevalence of the G1691A mutation in the factor V gene (factor V Leiden) and the G20210A prothrombin gene mutation in the Thai population
rs3136516
Role of prothrombin 19911 A>G polymorphism, blood group and male gender in patients with venous thromboembolism: Results of a German cohort study
rs1799963
The Prevalence of the Prothrombin (F2) 20210G>A Mutation in a Cohort of Sri Lankan Patients with Thromboembolic Disorders