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Early onset atrial fibrillation

PPFIA4 · rs3737883

Where this position leads

Condition: Atrial Fibrillation

rs3737883 Condition: Atrial Fibrillation Atrial Fibrillation Condition rs3737883 rs3737883 PPFIA4

What the study found

Who was studied 672 Korean ancestry cases, 3,700 Korean ancestry controls; replicated in 200 Korean ancestry cases, 1,812 Korean ancestry controls.

The effect Each copy of the A allele carried 1.48 times the odds of Early onset atrial fibrillation (95% confidence interval 1.31-1.68); p = 2 × 10−9.

How common The A allele had a frequency of about 68% in the people studied.

Where it sits Chromosome 1, band 1q32.1 — in an intron of LOC105371687.

What each result means

A/A Two copies of the version the research linked to Early onset atrial fibrillation. 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 Early onset atrial fibrillation. That is a smaller link than two copies.
G/G No copy of the version the research linked to Early onset atrial fibrillation. This is the starting point the study compared everyone against.
Source

Questions about rs3737883

What is rs3737883?

rs3737883 is a single position in the genome, in or near the PPFIA4 gene. Published research associates it with early onset atrial fibrillation. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs3737883 linked to?

On MyGeneLog this position is linked to Atrial Fibrillation. The research behind each link, and its sources, are set out on that condition page.

Does having rs3737883 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 rs3737883 come from?

GWAS Catalog, Eur Heart J 2017, PMID:28460022. 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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Early onset atrial fibrillation (rs3737883). MyGeneLog™. https://www.mygenelog.com/variants/rs3737883

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