Standard

systolic blood pressure (SBP, maximum, inv-normal transformed)

near FOXP1 · rs13092463

Where this position leads

Condition: Blood Pressure

rs13092463 Condition: Blood Pressure Blood Pressure Condition rs13092463 rs13092463 near FOXP1

What the study found

Who was studied 119,334 African American or Afro-Caribbean individuals, 57,991 Hispanic or Latin American individuals, 6,422 East Asian ancestry individuals, 425,750 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0203 higher (95% confidence interval 0.014-0.026); p = 2 × 10−11.

How common The G allele had a frequency of about 75% in the people studied.

Where it sits Chromosome 3, band 3p13 — between genes, 44.1 kb from FOXP1.

What each result means

A/A No copy of the version the research linked to systolic blood pressure (SBP, maximum, inv-normal transformed). This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to systolic blood pressure (SBP, maximum, inv-normal transformed). That is a smaller link than two copies.
G/G Two copies of the version the research linked to systolic blood pressure (SBP, maximum, inv-normal transformed). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs13092463

What is rs13092463?

rs13092463 is a single position in the genome, in or near the near FOXP1 gene. Published research associates it with systolic blood pressure (sbp, maximum, inv-normal transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs13092463 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 rs13092463 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 rs13092463 come from?

GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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 (SBP, maximum, inv-normal transformed) (rs13092463). MyGeneLog™. https://www.mygenelog.com/variants/rs13092463

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