Sensitive

Cardioembolic stroke (MTAG)

KCNJ5-AS1 · rs74399915

Where this position leads

Condition: Cardioembolic Stroke

rs74399915 Condition: Cardioembolic Stroke Cardioembolic Stroke Condition rs74399915 rs74399915 KCNJ5-AS1

What the study found

Who was studied 362,661 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 8.03 z score higher; p = 1 × 10−15.

Where it sits Chromosome 11, band 11q24.3 — in an intron of KCNJ5-AS1.

What each result means

C/C No copy of the version the research linked to Cardioembolic stroke (MTAG). This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Cardioembolic stroke (MTAG). That is a smaller link than two copies.
T/T Two copies of the version the research linked to Cardioembolic stroke (MTAG). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs74399915

What is rs74399915?

rs74399915 is a single position in the genome, in or near the KCNJ5-AS1 gene. Published research associates it with cardioembolic stroke (mtag). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs74399915 linked to?

On MyGeneLog this position is linked to Cardioembolic Stroke. The research behind each link, and its sources, are set out on that condition page.

Does having rs74399915 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 rs74399915 come from?

GWAS Catalog, Frontiers in cardiovascular medicine 2022, PMID:35872910. 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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Cardioembolic stroke (MTAG) (rs74399915). MyGeneLog™. https://www.mygenelog.com/variants/rs74399915

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