ReadYourDNA

Repaglinide (Prandin)

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

About Repaglinide

What it is

Repaglinide is a meglitinide: like the sulfonylureas, it closes potassium channels in the insulin-making beta cells of the pancreas, but it acts quickly and briefly, so it is taken with meals to cover the rise in blood sugar after eating. It is used for type 2 diabetes. It is sold as Prandin and NovoNorm, among other names.

How genes come into it

Repaglinide is taken into the liver by the transporter SLCO1B1 and broken down by CYP2C8 and CYP3A4. The SLCO1B1 variant rs4149056 raises its levels markedly, and some CYP2C8 versions change them too. Studies have also looked at diabetes genes such as KCNQ1, KCNJ11 and IGF2BP2 for how well it lowered blood sugar. The findings come from single or a few studies, and there is no CPIC or DPWG guideline.

What research found

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

Rated evidence (17 rated variants)

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

SLCO1B1 rs4149056: Level 3. Efficacy. 2.

SLCO1B1 rs2306283: Level 3. Other. 1.

KCNJ11 rs5219: Level 3. Efficacy: Diabetes Mellitus, Type 2. 1.

CYP2C8 rs10509681: Level 3. Other. 1.

Metabolism (6 findings)

Studies of how quickly the body processes this medication.

NR1I2 rs2276706: Genotype GG is associated with decreased metabolism of repaglinide in men as compared to genotype AA.

NR1I2 rs2276706: Genotype GG is associated with increased metabolism of repaglinide in men as compared to genotype AA.

NR1I2 rs3814058: Genotype CC is associated with decreased metabolism of repaglinide in men as compared to genotype TT.

NR1I2 rs3814058: Genotype CC is associated with increased metabolism of repaglinide in men as compared to genotype TT.

Response (7 findings)

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

KCNJ11 rs5219: Allele T is associated with increased response to repaglinide in people with Diabetes Mellitus, Type 2 as compared to genotype CC.

KCNQ1 rs2237892: Genotypes CT + TT are associated with increased response to repaglinide in people with Diabetes Mellitus, Type 2 as compared to genotype CC.

KCNQ1 rs2237895: Genotypes AC + CC are associated with increased response to repaglinide in people with Diabetes Mellitus, Type 2 as compared to genotype AA.

SLC30A8 rs13266634: Genotypes CT + TT are associated with increased response to repaglinide in people with Diabetes Mellitus, Type 2 as compared to genotype CC.

Dosing (5 findings)

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

CYP2C8 rs10509681: Allele C is associated with increased metabolism of repaglinide in healthy individuals as compared to allele T.

CYP2C8 rs11572080: Allele T is associated with increased metabolism of repaglinide in healthy individuals as compared to allele C.

IGF2BP2 rs1470579: Genotypes AC + CC are associated with decreased response to repaglinide in people with Diabetes Mellitus, Type 2 as compared to genotype AA.

IGF2BP2 rs4402960: Genotypes GT + TT are associated with increased response to repaglinide in people with Diabetes Mellitus, Type 2 as compared to genotype GG.

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

Actos (Thiazolidinediones)

Amaryl (Sulfonylureas)

Antithyroid Drugs (class) (Antithyroid Agents)

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.

Back to Medications

Content updated September 2026.

ReadYourDNA provides educational interpretation of DNA data you already have. It is not diagnostic, not a substitute for professional medical advice, diagnosis, or treatment, and is not intended to diagnose, treat, cure, or prevent any disease. Talk to a clinician before acting on any result.

Raw DNA Data Reports for 23andMe & AncestryDNA · About ReadYourDNA · FAQ · Methodology & Science · Pricing · Support and complaints · Legal & Contact · Health Traits · Pharmacogenomics · Carrier Status · Variant Explorer · The Human Karyotype · Privacy Policy · Terms of Service · Accessibility · Consumer Health Data Privacy · Your Privacy Choices · Editorial Standards · Your Data, Checkable · Sample Report · ReadYourDNA and Promethease compared · What is inside a 23andMe raw data file · What is inside an AncestryDNA raw data file · What a chatbot can and cannot do with your raw DNA file · Where a raw DNA file can still be uploaded in 2026

Written, maintained and operated by Martin Pechhacker, sole proprietor, Vienna, Austria. Trade register GISA 40064420. support@readyourdna.com