MTHFR DNA Wellness Report
In this report, we cover the MTHFR gene, analyze your genotypes for the rs1801133 and rs1801131 SNPs, and assess your general risk due to these MTHFR variants. We also use this analysis to make personalized, actionable health recommendations based on your unique genetic data.
MTHFR is the most talked-about gene among health enthusiasts and functional medicine practitioners. It’s also the best-studied gene in nutrigenetics, the science of how genes affect nutritional status. Short for methylenetetrahydrofolate reductase, MTHFR influences folate levels and methylation in your body. MTHFR became such a popular topic after large-scale studies linked poor methylation with chronic health problems. However, many claims about the impact of MTHFR are inflated. People have pinned virtually every problem on MTHFR, leading to a widespread misunderstanding of this gene.
In this report, we cover the main SNPs in the MTHFR gene: rs1801133 and rs1801131.You will get to understand how your MTHFR genotype can affect your health, and what you can do to lower your risk of chronic diseases and nutrient deficiencies. You may be surprised to hear that you might be better off avoiding methylation supplements even if you have the “bad” MTHFR variants.
This app analyzes your DNA data with a focus on the MTHFR gene and its impact upon your health.
Once your DNA data is stored in your Sequencing.com account, after purchasing this DNA report simply click the app's 'Start' button and you'll receive your report in about 30 minutes.
If your DNA data is not already stored in your account, you can either import your data from a DNA test you've already taken (such as from 23andMe or AncestryDNA) or you can order one of our DNA tests.
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|Our Universal DNA Compatibility enables this app to work with DNA data from almost any genetic test including 23andMe, Ancestry, MyHeritage, FTDNA, and genome sequencing.||Our clinical-grade 30x Whole Genome Sequencing test obtains data on 100% of your genome.|
Free DNA Data Upload
This DNA analysis report is compatible with data from almost all DNA tests and genome sequencing services.
|Test Compatibility||Format Compatibility||Variant Compatibility||Reference Genome Compatibility|
|Whole Genome Sequencing||FASTQ and FQ||SNP / SNV
(Single Nucleotide Variants)
|hg38 / GRCh38|
|Exome Sequencing||FASTA and FA||hg19 / GRCh37|
|Ultimate DNA Test||BAM||hg18 / GRCh36|
|23andMe||SAM||hg17 / GRCh35|
|Dante Labs||Genome VCF (gVCF and GVCF)|
|Genes for Good||CSV|
|HomeDNA||gz and zip compressed files|
|FTDNA||almost all other genetic data formats|
|New Amsterdam Genomics|
|almost all other genetic tests|
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The genetic analysis and statements that appear in this app, assessment and report have not been evaluated by the United States Food and Drug Administration. The Sequencing.com website and all software applications (Apps) that use Sequencing.com's website, as well as Sequencing.com's open Application Programming Interface (API), are not intended to diagnose, monitor, treat, cure, prevent nor alleviate any disease.