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P wave duration

CAV1 · rs3801995

What the study found

Who was studied 37,678 European ancestry individuals, 6,778 African ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.6 ms higher (95% confidence interval 0.42-0.78); p = 1 × 10−10.

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

Where it sits Chromosome 7, band 7q31.2 — in an intron of CAV1.

What each result means

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

Questions about rs3801995

What is rs3801995?

rs3801995 is a single position in the genome, in or near the CAV1 gene. Published research associates it with p wave duration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs3801995 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 rs3801995 come from?

GWAS Catalog, Circ Cardiovasc Genet 2017, PMID:28794112. 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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P wave duration (rs3801995). MyGeneLog™. https://www.mygenelog.com/variants/rs3801995

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