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B-type natriuretic peptide levels

NPPB · rs198389

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of B-type natriuretic peptide levels — no copies of the reported risk allele.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with B-type natriuretic peptide levels.
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of B-type natriuretic peptide levels compared to the general population.
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.

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