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Omeprazole (Prilosec)

Raw research findings for this medication. Mostly single studies, not curated or confirmed robust.

About Omeprazole

What it is

Omeprazole was the first proton pump inhibitor (PPI): it switches off the pumps in the stomach lining that release acid. It is used for heartburn and acid reflux, for stomach and duodenal ulcers, and as part of the treatment that clears Helicobacter pylori. It is sold as Prilosec and Losec, among other names, and in many countries without prescription.

How genes come into it

Omeprazole is broken down mainly by the liver enzyme CYP2C19, and its blood levels differ several-fold between people with different gene versions. Poor and intermediate metabolizers keep it longer and their stomach acid stays lower, which studies link to better ulcer healing and Helicobacter cure; people with the fast *17 version clear it more quickly. CPIC and DPWG have published guidelines on CYP2C19 and omeprazole, and the US FDA lists an effect on drug levels. A few other genes such as IL1B have been studied, with weaker evidence.

Published guidelines

Clinical guidelines that name a gene for Omeprazole. They sort people into groups by the gene copies they carry.

CPIC guideline: CYP2C19. Ultrarapid Metabolizer · Rapid Metabolizer · Normal Metabolizer · Likely Intermediate Metabolizer · Intermediate Metabolizer · Likely Poor Metabolizer · Poor Metabolizer · Indeterminate. Moderate. 2021.

DPWG guideline: CYP2C19. Ultrarapid Metabolizer · Rapid Metabolizer · Normal Metabolizer · Likely Intermediate Metabolizer · Intermediate Metabolizer · Likely Poor Metabolizer · Poor Metabolizer · Indeterminate. 2011.

US FDA: CYP2C19. Likely Intermediate Metabolizer · Intermediate Metabolizer · Likely Poor Metabolizer · Poor Metabolizer. Data that Demonstrate a Potential Impact on Pharmacokinetic Properties Only.

What research found

Every published finding on gene variants and Omeprazole. Upload your DNA file to see which of these rows apply to you.

Rated evidence (5 rated variants)

PharmGKB weighs all studies of a variant and rates how strong the evidence is, from 1A (strongest) to 4.

CYP2C19 CYP2C19*1, CYP2C19*2, CYP2C19*3, CYP2C19*9, CYP2C19*10, CYP2C19*17, CYP2C19*24, CYP2C19*26: Level 1A · replicated. Metabolism/PK: Gastroesophageal Reflux. 28.

CYP2C19 CYP2C19*1, CYP2C19*2, CYP2C19*3: Level 1A · replicated. Efficacy: Esophagitis, Gastroesophageal Reflux, Helicobacter Infections, Peptic Ulcer Disease. 27.

IL1B rs16944: Level 3. Efficacy: Helicobacter Infections. 3.

CYP2C19 CYP2C19*1, CYP2C19*23, CYP2C19*29, CYP2C19*30, CYP2C19*31, CYP2C19*33: Level 3. Metabolism/PK. 2.

Metabolism (38 findings)

Studies of how quickly the body processes this medication.

rs12777823: Allele A is associated with increased concentrations of 5-hydroxyomeprazole and omeprazole in healthy individuals as compared to allele G.

ABCB1 rs1045642: Genotypes AA + AG are associated with increased concentrations of omeprazole in infants with Gastroesophageal Reflux as compared to genotype GG.

CYP2C19 CYP2C19 poor metabolizers: CYP2C19 poor metabolizer is associated with decreased metabolism of omeprazole in healthy individuals as compared to CYP2C19 normal metabolizer.

CYP2C19 CYP2C19 poor metabolizers: CYP2C19 poor metabolizer is associated with decreased metabolism of omeprazole in healthy individuals as compared to CYP2C19 normal metabolizer.

Response (67 findings)

Studies of how well it worked in people carrying a variant.

ABCB1 rs1045642: Genotype AA is associated with increased response to omeprazole or pantoprazole in people with Helicobacter Infections as compared to genotypes AG + GG.

CYP2C19 CYP2C19 normal metabolizer genotype: CYP2C19 normal metabolizer is associated with decreased clinical benefit to amoxicillin, clarithromycin and omeprazole in people with Helicobacter Infections as compared to CYP2C19 poor metabolizer.

CYP2C19 CYP2C19 poor metabolizer and intermediate metabolizer genotypes: CYP2C19 intermediate metabolizer and poor metabolizer is associated with increased clinical benefit to lansoprazole or omeprazole in people with Helicobacter Infections as compared to CYP2C19 normal metabolizer.

CYP2C19 CYP2C19*1, CYP2C19*2: CYP2C19 *1/*2 is associated with increased response to omeprazole or pantoprazole in people with Helicobacter Infections as compared to CYP2C19 *1/*1.

Dosing (2 findings)

Studies of how much of the drug people needed or tolerated.

CYP2C19 rs11188072: Genotype TT is associated with increased metabolism of omeprazole in people with no disease as compared to genotype CC.

CYP2C19 rs12248560: Genotype TT is associated with increased metabolism of omeprazole in people with no disease as compared to genotype CC.

Study findings and evidence levels: PharmGKB (CC BY-SA 4.0). Guidelines: CPIC and DPWG, as bundled in PharmCAT. Most studies were done mainly in people of European ancestry.

Related Drugs

More drugs from the same category

Aciphex (PPIs)

Dexilant (PPIs)

Nexium (PPIs)

Not a prescribing recommendation. This page is educational information about pharmacogenomic research and clinical guidelines - it is not medical or dosing advice, and not a prediction of how any medication will work for you. Never start, stop, or change a medication or dose based on it; talk to your doctor or pharmacist, who can order clinical-grade testing if appropriate.

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Content updated September 2026.

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