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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 33,955 European ancestry individuals, 6,778 African individuals.
The effect
Each copy of the A allele shifted the measure 244 ms x uV higher (95% confidence interval 163.64-324.36); p = 3 × 10−9.
How common The A allele had a frequency of about 11% in the people studied.
Where it sits Chromosome 4, band 4q28.3 — in an intron of LINC02511.
What each result means
A/ATwo copies of the version the research linked to P wave terminal force. 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 P wave terminal force. That is a smaller link than two copies.
G/GNo copy of the version the research linked to P wave terminal force. This is the starting point the study compared everyone against.
rs11099412 is a single position in the genome, in or near the PCDH18 gene. Published research associates it with p wave terminal force. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs11099412 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 rs11099412 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.
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Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
P wave terminal force (rs11099412). MyGeneLog™. https://www.mygenelog.com/variants/rs11099412