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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 104 Japanese ancestry cases, 46,527 Japanese ancestry controls.
The effect
Each copy of the G allele carried 31.50 times the odds of Arrhythmogenic cardiomyopathy (95% confidence interval 19.2-51.9); p = 2 × 10−42.
How common The G allele had a frequency of about 1% in the people studied.
Where it sits Chromosome 18, band 18q12.1 — in an intron of DSG4.
What each result means
A/ANo copy of the version the research linked to Arrhythmogenic cardiomyopathy. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Arrhythmogenic cardiomyopathy. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Arrhythmogenic cardiomyopathy. That is the strongest link of the three results. A link in a study is not a diagnosis.
Journal of arrhythmia · 2026 · PMID 41607864 · open access
Questions about rs182626537
What is rs182626537?
rs182626537 is a single position in the genome, in or near the DSG4 gene. Published research associates it with arrhythmogenic cardiomyopathy. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs182626537 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 rs182626537 come from?
GWAS Catalog, Journal of arrhythmia 2026, PMID:41607864. 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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