Standard

diastolic blood pressure (DBP, maximum, inv-normal transformed)

LINC02742 · rs78014576

Where this position leads

Condition: Blood Pressure

rs78014576 Condition: Blood Pressure Blood Pressure Condition rs78014576 rs78014576 LINC02742

What the study found

Who was studied 119,274 African American or Afro-Caribbean individuals, 57,979 Hispanic or Latin American individuals, 6,421 East Asian ancestry individuals, 425,680 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0219 lower (95% confidence interval 0.015-0.028); p = 4 × 10−11.

How common The T allele had a frequency of about 82% in the people studied.

Where it sits Chromosome 11, band 11p14.1 — in an intron of LINC02742.

What each result means

A/A No copy of the version the research linked to diastolic blood pressure (DBP, maximum, inv-normal transformed). This is the starting point the study compared everyone against.
A/T One copy of the version the research linked to diastolic blood pressure (DBP, maximum, inv-normal transformed). That is a smaller link than two copies.
T/T Two copies of the version the research linked to diastolic blood pressure (DBP, 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 rs78014576

What is rs78014576?

rs78014576 is a single position in the genome, in or near the LINC02742 gene. Published research associates it with diastolic blood pressure (dbp, 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 rs78014576 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 rs78014576 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 rs78014576 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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diastolic blood pressure (DBP, maximum, inv-normal transformed) (rs78014576). MyGeneLog™. https://www.mygenelog.com/variants/rs78014576

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