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Right ventricular ejection fraction

FHOD3 · rs501740

What the study found

Who was studied 29,488 European ancestry individuals; replicated in 12,307 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.054 higher (95% confidence interval 0.038-0.07); p = 5 × 10−11.

How common The G allele had a frequency of about 26% in the people studied.

Where it sits Chromosome 18, band 18q12.2 — in an intron of FHOD3.

What each result means

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

Questions about rs501740

What is rs501740?

rs501740 is a single position in the genome, in or near the FHOD3 gene. Published research associates it with right ventricular ejection fraction. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs501740 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 rs501740 come from?

GWAS Catalog, Nature genetics 2022, PMID:35697868. 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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Right ventricular ejection fraction (rs501740). MyGeneLog™. https://www.mygenelog.com/variants/rs501740

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