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Creatine kinase levels

CKM · rs11559024

What the study found

Who was studied 63,159 Icelandic ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.446 lower; p = 2 × 10−115.

How common The C allele had a frequency of about 2% in the people studied.

Where it sits Chromosome 19, band 19q13.32 — a missense change in CKM.

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Creatine kinase levels compared to the general population.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Creatine kinase levels.
T/T Published research associates this genotype with typical/baseline likelihood of Creatine kinase levels — no copies of the reported risk allele.
Source

Questions about rs11559024

What is rs11559024?

rs11559024 is a single position in the genome, in or near the CKM gene. Published research associates it with creatine kinase levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11559024 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 rs11559024 come from?

GWAS Catalog, Nature communications 2016, PMID:26838040. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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.

Creatine kinase levels (rs11559024). MyGeneLog™. https://www.mygenelog.com/variants/rs11559024

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