HelixlyAI Genome Report Prepared for Sample Subject
Report ID HX-2026-0042 · synthetic
Methylation & Metabolism · Document 07 of 24

MTHFR / Methylation

How Sample Subject's methylation-cycle variants are predicted to influence folate processing and homocysteine balance. All values below are synthetic.

3 findings1 Tier 1Reviewed 2026-01-15

Provenance

Data Provenanceverified chain
Document
MTHFR / Methylation
Source assembly
GRCh37 (hg19)
Source file SHA-256
0000a1b2c3d4e5f6…4b5c6d7e
Supersedes
prior v1 · SHA 1111f0e9…
Evidence sources
CPIC, dbSNP, PubMed
Access date
2026-01-15

Provider Alert

Considerations — Provider Ready3 items · discuss before supplementing
ConsiderationGene / GenotypeEvidenceRecommendationSource
Folate formMTHFR
(rs0067701 CT)
StrongReduced activity — discuss active 5-MTHF vs. folic acid with clinician.PubMed ↗
HomocysteineMTHFR / MTRModerateConsider baseline homocysteine testing to contextualize findings.PubMed ↗
B12 statusMTRR
(rs0067901 AG)
LimitedMonitor B12 if supplementing folate; combined support may be relevant.dbSNP ↗

Per-Gene Findings

Filter:

MTHFR — Reduced Activity

Methylenetetrahydrofolate reductase · folate cycle
StrongTier 1
rs00677011:11,800,000CT

Sample Subject carries one reduced-activity allele, predicting roughly 60–70% of reference enzyme activity. This is associated with modestly elevated homocysteine and altered folate processing in some individuals.

Historical contextPrior analysis (v1) reported this variant against an unspecified assembly; re-called here on GRCh37 with concordant genotype.

MTR — Normal Function

Methionine synthase · remethylation
ModerateTier 2
rs00678011:237,000,000AA

Reference genotype predicting normal methionine synthase function. No remethylation-pathway concern is indicated from this locus.

MTRR — Reduced Recycling

Methionine synthase reductase · B12 recycling
LimitedTier 2
rs00679015:7,900,000AG

Heterozygous genotype associated with mildly reduced B12 recycling. Clinical impact is uncertain and likely small in isolation.

Genotype Table

Variants evaluated in this document — synthetic
rsIDchr:posGenotypeGeneSignificance
rs00677011:11,800,000CTMTHFRTier 1
rs00678011:237,000,000AAMTRTier 2
rs00679015:7,900,000AGMTRRTier 2
Consult your prescribing clinician. This HelixlyAI report is a synthetic demonstration generated from a consumer DNA export. Every name, identifier, rsID, genotype, and citation shown is fictional. It is not a diagnosis or medical advice — do not start, stop, or change any medication or treatment based on this document.