Standard

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

NEURL4 · rs118077107

Where this position leads

Condition: Blood Pressure

rs118077107 Condition: Blood Pressure Blood Pressure Condition rs118077107 rs118077107 NEURL4

What the study found

Who was studied 425,750 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0682 higher (95% confidence interval 0.054-0.082); p = 3 × 10−21.

How common The C allele had a frequency of about 97% in the people studied.

Where it sits Chromosome 17, band 17p13.1 — a missense change in NEURL4.

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 rs118077107

What is rs118077107?

rs118077107 is a single position in the genome, in or near the NEURL4 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 rs118077107 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 rs118077107 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 rs118077107 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) (rs118077107). MyGeneLog™. https://www.mygenelog.com/variants/rs118077107

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