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Aortic valve area

FER · rs113193866

What the study found

Who was studied 59,569 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0923 lower (95% confidence interval 0.072-0.112); p = 1 × 10−19.

How common The A allele had a frequency of about 92% in the people studied.

Where it sits Chromosome 5, band 5q21.3 — in an intron of FER.

What each result means

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

Questions about rs113193866

What is rs113193866?

rs113193866 is a single position in the genome, in or near the FER gene. Published research associates it with aortic valve area. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs113193866 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 rs113193866 come from?

GWAS Catalog, Nature genetics 2026, PMID:41419685. 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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Aortic valve area (rs113193866). MyGeneLog™. https://www.mygenelog.com/variants/rs113193866

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