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Right ventricular ejection fraction

OBSCN · rs78529941

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 0.05 higher (95% confidence interval 0.034-0.066); p = 1 × 10−10.

How common The G allele had a frequency of about 62% in the people studied.

Where it sits Chromosome 1, band 1q42.13 — in an intron of OBSCN.

What each result means

A/A No copy of the version the research linked to Right ventricular ejection fraction. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Right ventricular ejection fraction. That is a smaller link than two copies.
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.
Source

Questions about rs78529941

What is rs78529941?

rs78529941 is a single position in the genome, in or near the OBSCN 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 rs78529941 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 rs78529941 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 (rs78529941). MyGeneLog™. https://www.mygenelog.com/variants/rs78529941

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