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Who was studied 216 Korean ancestry cases, 296 Korean ancestry controls.
The effect
Each copy of the A allele carried 9.80 times the odds of Moyamoya disease (95% confidence interval 5.68-16.92); p = 3 × 10−16.
How common The A allele had a frequency of about 6% in the people studied.
Where it sits Chromosome 6, band 6p21.33 — in a non-coding transcript of EHMT2.
What each result means
A/ATwo copies of the version the research linked to Moyamoya disease. 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 Moyamoya disease. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Moyamoya disease. This is the starting point the study compared everyone against.
rs3869145 is a single position in the genome, in or near the EHMT2 gene. Published research associates it with moyamoya disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs3869145 linked to?
On MyGeneLog this position is linked to Moyamoya Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs3869145 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 rs3869145 come from?
GWAS Catalog, Journal of human genetics 2023, PMID:37365321. 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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