Symptomatic extra- and intra-cranial atherosclerotic stenosis
near OR1S2 · rs866262287
0 422Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others2Total4Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
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 9,947 Han Chinese ancestry individuals, 294 individuals.
The effect
Each copy of the G allele shifted the measure 0.86 higher (95% confidence interval 0.62-1.1); p = 2 × 10−13.
Where it sits Chromosome 11, band 11q12.1 — between genes, 4 kb from OR1S2.
What each result means
A/ANo copy of the version the research linked to Symptomatic extra- and intra-cranial atherosclerotic stenosis. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Symptomatic extra- and intra-cranial atherosclerotic stenosis. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Symptomatic extra- and intra-cranial atherosclerotic stenosis. That is the strongest link of the three results. A link in a study is not a diagnosis.
Cell discovery · 2023 · PMID 37479695 · open access
Questions about rs866262287
What is rs866262287?
rs866262287 is a single position in the genome, in or near the near OR1S2 gene. Published research associates it with symptomatic extra- and intra-cranial atherosclerotic stenosis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs866262287 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 rs866262287 come from?
GWAS Catalog, Cell discovery 2023, PMID:37479695. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 422Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others2Total4Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
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.
Symptomatic extra- and intra-cranial atherosclerotic stenosis (rs866262287). MyGeneLog™. https://www.mygenelog.com/variants/rs866262287