Standard

Systolic blood pressure

EEPD1 · rs62447769

Where this position leads

Condition: Blood Pressure

rs62447769 Condition: Blood Pressure Blood Pressure Condition rs62447769 rs62447769 EEPD1

What the study found

Who was studied 507,850 East Asian ancestry individuals, 420,829 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0237 higher (95% confidence interval 0.017-0.031); p = 3 × 10−11.

Where it sits Chromosome 7, band 7p14.2 — in an intron of EEPD1.

What each result means

A/A Two copies of the version the research linked to Systolic blood pressure. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Systolic blood pressure. That is a smaller link than two copies.
G/G No copy of the version the research linked to Systolic blood pressure. This is the starting point the study compared everyone against.
Source

Questions about rs62447769

What is rs62447769?

rs62447769 is a single position in the genome, in or near the EEPD1 gene. Published research associates it with systolic blood pressure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs62447769 linked to?

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

Does having rs62447769 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 rs62447769 come from?

GWAS Catalog, Nature communications 2025, PMID:40436827. 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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Systolic blood pressure (rs62447769). MyGeneLog™. https://www.mygenelog.com/variants/rs62447769

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