HelixlyAI Genome Report Prepared for Sample Subject
Report ID HX-2026-0042 · synthetic
Pharmacology · Document 05 of 24

Drug Metabolism (CYP450)

Sample Subject's cytochrome P450 metabolizer status across the major drug-metabolizing enzyme families, with provider-ready, evidence-graded recommendations. All values below are synthetic and for demonstration only.

7 findings 3 Tier 1 6 CPIC Level A Reviewed 2026-01-15

Provenance

Data Provenance verified chain
Document
Drug Metabolism (CYP450)
Source assembly
GRCh37 (hg19)
Source file SHA-256
0000a1b2c3d4e5f6…4b5c6d7e
Supersedes
prior v1 · SHA 1111f0e9…
Evidence sources
CPIC, PharmGKB, dbSNP, PubMed
Access date
2026-01-15

Provider Alert

Actionable Findings — Provider Ready 5 drugs · review before prescribing
DrugGene / GenotypeEvidenceRecommendationSource
Codeine CYP2D6
(rs3892097 AA)
CPIC Level A Poor metabolizer; codeine provides inadequate analgesia; select a non-CYP2D6 analgesic. Consult your prescribing clinician. CPIC ↗
Clopidogrel CYP2C19
(rs4244285 GA)
CPIC Level A Intermediate metabolizer; reduced activation of clopidogrel; an alternative antiplatelet agent is appropriate. Consult your prescribing clinician. CPIC ↗
Warfarin CYP2C9 + VKORC1
(rs1799853 CT / rs9923231 TT)
CPIC Level A Increased sensitivity; a reduced initiation dose with INR monitoring maintains target INR. Consult your prescribing clinician. CPIC ↗
Tacrolimus CYP3A5
(rs776746 GG)
CPIC Level A Non-expresser; standard per-kg dosing reaches target troughs. Consult your prescribing clinician. CPIC ↗
Fluorouracil DPYD
(rs3918290 CC)
CPIC Level A Normal DPD activity; standard fluoropyrimidine dosing applies. Consult your prescribing clinician. CPIC ↗

Per-Gene Findings

Filter:

CYP2D6 — Poor Metabolizer

Cytochrome P450 2D6 · enzyme activity
CPIC Level ATier 1
rs3892097 22:42,524,947 AA

Two no-function alleles define a poor metabolizer phenotype. Standard doses of CYP2D6 substrates produce elevated exposure relative to normal metabolizers.

CYP2C19 — Intermediate Metabolizer

Cytochrome P450 2C19 · prodrug activation
CPIC Level ATier 1
rs4244285 10:96,541,616 GA

One loss-of-function allele defines an intermediate metabolizer phenotype, which reduces activation of clopidogrel to its active form.

CYP2C9 — Reduced Function

Cytochrome P450 2C9 · warfarin clearance
CPIC Level ATier 1
rs1799853 10:96,702,047 CT

One reduced-function allele lowers warfarin clearance. A lower maintenance dose maintains the target INR for this genotype.

CYP3A5 — Non-expresser

Cytochrome P450 3A5 · tacrolimus exposure
CPIC Level ATier 2
rs776746 7:99,270,539 GG

The GG genotype defines a non-expresser. Standard per-kilogram tacrolimus dosing reaches target trough concentrations.

CYP1A2 — Intermediate Metabolizer

Cytochrome P450 1A2 · caffeine clearance
PharmGKBTier 2
rs762551 15:75,041,917 AC

The AC genotype defines intermediate caffeine metabolism, with slower clearance than the AA (rapid) genotype.

VKORC1 — High Warfarin Sensitivity

Vitamin K epoxide reductase · warfarin target
CPIC Level ATier 2
rs9923231 16:31,107,689 TT

The TT genotype confers high warfarin sensitivity. A low initiation dose is appropriate for this genotype.

DPYD — Normal Activity

Dihydropyrimidine dehydrogenase · fluoropyrimidine clearance
CPIC Level ATier 3
rs3918290 1:97,915,614 CC

The CC (reference) genotype defines normal DPD activity. Standard fluoropyrimidine dosing applies for this genotype.

Genotype Table

Variants evaluated in this document — synthetic
rsIDchr:posGenotypeGeneSignificance
rs389209722:42,524,947AACYP2D6Tier 1
rs424428510:96,541,616GACYP2C19Tier 1
rs179985310:96,702,047CTCYP2C9Tier 1
rs7767467:99,270,539GGCYP3A5Tier 2
rs76255115:75,041,917ACCYP1A2Tier 2
rs992323116:31,107,689TTVKORC1Tier 2
rs39182901:97,915,614CCDPYDTier 3
Consult your prescribing clinician. This HelixlyAI report is a synthetic demonstration generated from a consumer DNA export. It is not a diagnosis, prescription, or substitute for professional medical advice. Do not start, stop, or change any medication based on this document. Genotype is one of many factors influencing drug response.