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Who was studied 252,730 European ancestry, African ancestry, Hispanic or Latin American, South East Asian ancestry, South Asian ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0212 higher (95% confidence interval 0.015-0.027); p = 4 × 10−12.
How common The A allele had a frequency of about 47% in the people studied.
Where it sits Chromosome 16, band 16q12.2 — between genes, 47.2 kb from LINC02140.
What each result means
A/ATwo copies of the version the research linked to QRS duration. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to QRS duration. That is a smaller link than two copies.
G/GNo copy of the version the research linked to QRS duration. This is the starting point the study compared everyone against.
Nature communications · 2022 · PMID 36050321 · open access
Questions about rs7186341
What is rs7186341?
rs7186341 is a single position in the genome, in or near the near LINC02140 gene. Published research associates it with qrs duration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7186341 linked to?
On MyGeneLog this position is linked to Cardiac Conduction Intervals (PR Interval and QRS Duration). The research behind each link, and its sources, are set out on that condition page.
Does having rs7186341 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 rs7186341 come from?
GWAS Catalog, Nature communications 2022, PMID:36050321. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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