ENDOV · rs41301888
Where this position leads
Condition: Moyamoya Disease
What the study found
Who was studied 216 Korean ancestry cases, 296 Korean ancestry controls.
The effect Each copy of the T allele carried 9.64 times the odds of Moyamoya disease (95% confidence interval 5.95-15.6); p = 3 × 10−20.
How common The T allele had a frequency of about 16% in the people studied.
Where it sits Chromosome 17, band 17q25.3 — in an intron of ENDOV.
rs41301888 is a single position in the genome, in or near the ENDOV 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.
On MyGeneLog this position is linked to Moyamoya Disease. The research behind each link, and its sources, are set out on that condition page.
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.
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.
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.
Moyamoya disease (rs41301888). MyGeneLog™. https://www.mygenelog.com/variants/rs41301888