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Angiotensin-converting enzyme activity

ACE · rs4343

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Angiotensin-converting enzyme activity — no copies of the reported risk allele. (GWAS Catalog, Pharmacogenomics J 2010, PMID:20066004)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Angiotensin-converting enzyme activity. (GWAS Catalog, Pharmacogenomics J 2010, PMID:20066004)
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Angiotensin-converting enzyme activity compared to the general population. (GWAS Catalog, Pharmacogenomics J 2010, PMID:20066004)

Source: GWAS Catalog, Pharmacogenomics J 2010, PMID:20066004

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 rs4343

What is rs4343?

rs4343 is a single position in the genome, in or near the ACE gene. Published research associates it with angiotensin-converting enzyme activity. 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 rs4343?

Subjects that appear in the title or abstract of the same papers as this rsID include kidneys (4 papers), fertility (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 rs4343 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 rs4343 come from?

GWAS Catalog, Pharmacogenomics J 2010, PMID:20066004. 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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