Sensitive

Coronary artery disease (MTAG)

ZNF827 · rs10006310

Where this position leads

Condition: Coronary Artery Disease

rs10006310 Condition: Coronary Artery Disease Coronary Artery Disease Condition rs10006310 rs10006310 ZNF827

What the study found

Who was studied 310,368 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 6.35 z-score higher; p = 2 × 10−10.

How common The T allele had a frequency of about 53% in the people studied.

Where it sits Chromosome 4, band 4q31.21 — in an intron of ZNF827.

What each result means

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

Questions about rs10006310

What is rs10006310?

rs10006310 is a single position in the genome, in or near the ZNF827 gene. Published research associates it with coronary artery disease (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 rs10006310 linked to?

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

Does having rs10006310 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 rs10006310 come from?

GWAS Catalog, NPJ genomic medicine 2025, PMID:41022758. 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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Coronary artery disease (MTAG) (rs10006310). MyGeneLog™. https://www.mygenelog.com/variants/rs10006310

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