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Analgesic

Opioids

One of the most studied genes in all of pharmacogenomics sits here — and the guideline that reviewed it concluded that no dosing recommendation can be made. That conclusion is the finding.

Chemical structure of Opioids: morphine, drawn by MyGeneLog™ from PubChem records
Chemical structure of morphine, drawn by MyGeneLog™ from public PubChem records. Free to reuse under CC BY 4.0 with credit to MyGeneLog™.

What this drug connects to

Opioids Condition: Opioid Receptor Sensitivity (OPRM1) Opioid Receptor Sensitivity (OPRM1) Condition Variant: rs1799971 · OPRM1 rs1799971 · OPRM1 Variant Variant: rs696523 · OPRM1 rs696523 · OPRM1 Variant Variant: rs17181171 · OPRM1 rs17181171 · OPRM1 Variant Variant: rs3778150 · OPRM1 rs3778150 · OPRM1 Variant Variant: rs79910351 · OPRM1 rs79910351 · OPRM1 Variant Variant: +7 more +7 more Variant Topic: Alcohol and the flush Alcohol and the flush Topic Topic: Depression and stress Depression and stress Topic Topic: Smoking and vaping Smoking and vaping Topic Opioids Opioids Analgesic

Solid lines are connections this site curates. Dashed lines mean the two ends share a research paper — worth knowing, and not a claim that one explains the other.

The genes involved

OPRM1

Opioid Receptor Sensitivity (OPRM1) →

CPIC reviewed OPRM1 rs1799971 (A118G) for opioid therapy and issued no dosing recommendation. Some studies show a small (~10%) increase in postoperative morphine dose requirements in G-allele carriers, but CPIC concluded this effect is too modest to be clinically actionable. CPIC level C (insufficient evidence for a recommendation).

Crews KR, et al. Clinical Pharmacogenetics Implementation Consortium Guideline for CYP2D6, OPRM1, and COMT Genotypes and Select Opioid Therapy. Clin Pharmacol Ther. 2021;109(6):1420-1425. PMID 33387367.

OPRM1 (upstream locus)

Opioid Receptor Sensitivity (OPRM1) →

This is a second, separate OPRM1-region finding from the A118G variant already on this page — a different locus entirely, 306,000 bases upstream of the gene. In African-American participants being treated for opioid dependence with methadone (383 people), each copy of the minor allele corresponded to needing about 20mg more methadone per day (P = 2.8×10⁻⁸). The same effect was not found in 1,027 European-American participants in the same study — an ancestry-specific result, stated rather than generalised. It replicated in a different setting entirely: opioid-naive African-American children treated for surgical pain with the same allele needed a higher morphine dose. Two different opioids, two different clinical contexts, the same direction of effect.

Smith AH et al., Molecular Psychiatry 2017 — genome-wide association study of therapeutic opioid dosing identifies a novel locus upstream of OPRM1. PMID:28115739

In the news

2026-02-19 · Larisa H. Cavallari et al., IGNITE Network's ADOPT PGx Acute Pain Trial, published in JAMA Network Open (eight U.S. health systems)

CYP2D6-Guided Opioid Management and Postoperative Pain Control: A Randomized Clinical Trial

A large, multi-site pragmatic randomized trial (eight U.S. health systems) tested whether prescribing opioids based on CYP2D6 metabolizer phenotype improved post-surgical pain control for hydrocodone, oxycodone and tramadol, compared with usual care. It found no significant improvement -- an honest negative result from real clinical practice, not a lab study, and it directly matches what this page already says: a well-studied gene, and no dosing recommendation that follows from it.

Whose work this rests on

Every guideline above was written by people. Named here because they are contributors to this page in the same sense anybody else on this site is.

Variants MyGeneLog™ reports for these genes

These are the positions in your own file that carry the genes above. Not every gene in a guideline is one we report — where that is the case the gene appears above without a variant here, and the note says so.

Opioid receptor sensitivity

OPRM1 · rs1799971

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Testosterone levels

OPRM1 · rs696523

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Menstruation quality of life impact (fever)

OPRM1 · rs17181171

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Height

OPRM1 · rs3778150

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Height

OPRM1 · rs79910351

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Weight

OPRM1 · rs9688977

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Whole body water mass (UKB data field 23102)

OPRM1 · rs514980

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Opioid use disorder

OPRM1 · rs3778151

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Insulin-like growth factor 1 levels

OPRM1 · rs13193545

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Body mass index

OPRM1 · rs1294093

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Methadone dose in opioid dependence

OPRM1 · rs73568641

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Total testosterone levels

OPRM1 · rs7773995

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Questions about Opioids

What are opioids?

Opioids are pain-relieving medicines, including morphine. One of the most studied genes in all of pharmacogenomics — OPRM1 — sits here, and the guideline that reviewed it concluded that no dosing recommendation can be made.

Does the OPRM1 A118G variant mean I’ll need a different opioid dose?

Not according to current guidance. CPIC reviewed the OPRM1 rs1799971 (A118G) variant for opioid therapy and issued no dosing recommendation. Some studies find G-allele carriers need roughly 10% more morphine after surgery, but CPIC rated the evidence level C — real but too modest to act on.

What is the OPRM1 upstream locus finding for opioids?

A separate signal, about 306,000 bases from the OPRM1 gene itself, found in African-American patients treated for opioid dependence with methadone: each copy was linked to needing about 20mg more methadone per day across 383 people studied. The same effect wasn’t found in 1,027 European-American participants in that study.

Has the OPRM1 upstream locus finding been confirmed for other opioids?

Yes. Opioid-naive African-American children treated for surgical pain who carried the same allele needed higher morphine doses — a different opioid and a different clinical context pointing the same direction, though like the A118G variant it isn’t the basis of any dosing guideline.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Opioids. MyGeneLog™. https://www.mygenelog.com/drugs/opioids

This page is educational and contains no dosing information. Where a clinical guideline covers one of these gene-drug pairs it is written for prescribers and works through validated algorithms alongside clinical monitoring. Nothing here is a reason to start, stop, or change a medication — that conversation belongs with the clinician or pharmacist managing your treatment.