Sensitive

Plasma X-21471 levels in chronic kidney disease

SLCO1B1 · rs12318075

Where this position leads

Drugs: Statins, Ticagrelor

rs12318075 Drug: Statins Statins Drug Drug: Ticagrelor Ticagrelor Drug rs12318075 rs12318075 SLCO1B1

What the study found

Who was studied 3,964 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.306 higher (95% confidence interval 0.26-0.36); p = 6 × 10−32.

How common The G allele had a frequency of about 20% in the people studied.

Where it sits Chromosome 12, band 12p12.1 — in an intron of SLCO1B1.

What each result means

G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Plasma X-21471 levels in chronic kidney disease compared to the general population.
G/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Plasma X-21471 levels in chronic kidney disease.
T/T Published research associates this genotype with typical/baseline likelihood of Plasma X-21471 levels in chronic kidney disease — no copies of the reported risk allele.
Source

Questions about rs12318075

What is rs12318075?

rs12318075 is a single position in the genome, in or near the SLCO1B1 gene. Published research associates it with plasma x-21471 levels in chronic kidney disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does rs12318075 affect how medicines work?

SLCO1B1 carries pharmacogenomic findings for Statins, Ticagrelor. That is educational information, not a prescription or a dosing guide. Any decision to start, stop or change a medicine belongs with the clinician or pharmacist managing your treatment.

Does having rs12318075 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs12318075 come from?

GWAS Catalog, Nature genetics 2023, PMID:37277652. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Plasma X-21471 levels in chronic kidney disease (rs12318075). MyGeneLog™. https://www.mygenelog.com/variants/rs12318075

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