Pharmacogenomics
How the SLCO1B1 gene affects the way your body handles some statins, what published guidance says, what a genetic test can’t tell you, and what to ask.
By the GeneMatrix editorial teamUpdated 3 min read

In short
Some people carry SLCO1B1 variants that let certain statins build up in the blood, which is linked to a higher chance of muscle side effects. Published CPIC guidance tells prescribers how to use that result. A test can’t tell you whether you need a statin.
Pharmacogenomic results describe how your body is likely to process certain medicines. They do not tell you whether a medicine will work for you, and they are not dosing instructions. Never start, stop or change a medication because of a genetic result. Bring it to the prescriber who manages your medicines.
On this page
What is a statin genetic test?
Statins are cholesterol-lowering medicines. A statin genetic test is a pharmacogenomic (PGx) test, a kind of DNA test for medications, that reads a gene called SLCO1B1. It doesn’t tell you whether you need a statin. It describes how your body is likely to handle some of them, for the person who prescribes for you.
SLCO1B1 makes a transporter, a protein that carries statins from the blood into the liver, where they do their work. Some common variants make the transporter work less well, so more of certain statins stays in the blood. That is linked to a higher chance of statin-related muscle symptoms, such as aches or weakness.[1]
Which statins does SLCO1B1 affect?
CPIC’s 2022 statin guideline gives prescribers recommendations based on SLCO1B1 for several statins.[1] These three are in our Medication Check, each at CPIC level A:[2]
- Atorvastatin. Its guidance uses SLCO1B1.
- Simvastatin. Its guidance uses SLCO1B1.
- Rosuvastatin. Its guidance uses SLCO1B1. Its guidance also uses ABCG2, which our test does not check.
Pharmacogenomic results describe how your body is likely to process certain medicines. They do not tell you whether a medicine will work for you, and they are not dosing instructions. Never start, stop or change a medication because of a genetic result. Bring it to the prescriber who manages your medicines.
What does an SLCO1B1 result mean?
A SLCO1B1 result describes how well your transporter is likely to work, in CPIC’s terms: for example normal, decreased or poor function.[1] With decreased or poor function, more of some statins stays in your blood, and the guideline sets out how a prescriber can take that into account.
A decreased-function result doesn’t mean you will get muscle symptoms, and a normal result doesn’t mean you won’t. Other things play a part too, including your other medicines and your health.
What can’t a statin gene test tell you?
- Whether you need a statin. That rests on things a genetic test doesn’t read, and it is a decision for you and your clinician.
- Your health risks. It reads how you’re likely to handle some medicines, not your chance of any illness.
- Whether a statin will help you. It describes how your body is likely to handle one, not how well it will work.
- Whether you’ll have side effects. It shows one known influence on muscle symptoms, not what will happen to you.
What to ask your prescriber
Bring the report to whoever prescribes your statin, or to the clinician who has suggested one. Some questions to start with:
- Does my SLCO1B1 result matter for the statin I take, or one you are thinking about?
- Is there anything in my result you would want to keep an eye on?
- Which muscle symptoms should I tell you about?
Where GenePGx fits
GenePGx, our pharmacogenomic test, uses one saliva sample you collect at home. Checks selected known variants in 15 genes, plus CYP2D6 copy number, by genotyping. SLCO1B1 is among them, and your report sets its result beside the medicines whose guidance uses it. It tests genes named in CPIC prescribing guidelines for 56 medicines (checked September 29, 2026).
GenePGx is for adults 18 and older. To look up a single medicine first, use the Medication Check.
Sources
- [1]CPIC guideline for SLCO1B1, ABCG2, and CYP2C9 genotypes and statin-associated musculoskeletal symptoms. Clinical Pharmacology & Therapeutics, 2022. Accessed .
- [2]Genes-drugs: CPIC levels for each gene and drug pair. Clinical Pharmacogenetics Implementation Consortium, on ClinPGx. Accessed .
How we write and source these pieces: our editorial policy.
Related reading
- How does pharmacogenomics work? A plain-English guideSome genes change how quickly you process certain medicines, and published guidance says when that matters.Updated September 30, 2026
- Pharmacogenomics in 2026: what the evidence saysNearly everyone carries a gene variant that may change how their body processes a medicine. Here is what the evidence says in 2026.Updated October 1, 2026
- Do mental health DNA tests work? What they can and can’t tell you about psychiatric medicinesWhat a mental health DNA test reads, what it can’t tell you, and what the depression trials found.Updated September 30, 2026
