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B-type natriuretic peptide levels

NPPB · rs198389

What the study found

Who was studied 2,790 Black individuals.

The effect Each copy of the G allele shifted the measure 0.18 higher (95% confidence interval 0.12-0.24); p = 1 × 10−9.

How common The G allele had a frequency of about 40% in the people studied.

Where it sits Chromosome 1, band 1p36.22 — between genes, 0.2 kb from NPPB.

What each result means

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

What people read about alongside this

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs198389

What is rs198389?

rs198389 is a single position in the genome, in or near the NPPB gene. Published research associates it with b-type natriuretic peptide levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What do people read about alongside rs198389?

Subjects that appear in the title or abstract of the same papers as this rsID include heart and circulation (14 papers), blood sugar and insulin (5 papers), longevity and ageing (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs198389 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 rs198389 come from?

GWAS Catalog, Circ Cardiovasc Genet 2015, PMID:25561047. 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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B-type natriuretic peptide levels (rs198389). MyGeneLog™. https://www.mygenelog.com/variants/rs198389

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