Standard

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

EBF1 · rs2072495

Where this position leads

Condition: Blood Pressure

rs2072495 Condition: Blood Pressure Blood Pressure Condition rs2072495 rs2072495 EBF1

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 C allele shifted the measure 0.0226 lower (95% confidence interval 0.017-0.028); p = 2 × 10−17.

How common The C allele had a frequency of about 65% in the people studied.

Where it sits Chromosome 5, band 5q33.3 — in an intron of EBF1.

What each result means

C/C 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.
C/T 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.
T/T 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.
Source

Questions about rs2072495

What is rs2072495?

rs2072495 is a single position in the genome, in or near the EBF1 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 rs2072495 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 rs2072495 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 rs2072495 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) (rs2072495). MyGeneLog™. https://www.mygenelog.com/variants/rs2072495

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