2 525217233128Reads by AI crawlersClaude5ChatGPT2Google · Gemini0Perplexity1Meta AI7Microsoft · Copilot2Amazon3Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others28Total52Counted 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 12,531 European ancestry individuals; replicated in 8,216 Asian ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0803 higher (95% confidence interval 0.056-0.104); p = 5 × 10−11.
How common The A allele had a frequency of about 40% in the people studied.
Where it sits Chromosome 3, band 3q12.1 — in an intron of CMSS1.
What each result means
A/ATwo copies of the version the research linked to Axial length. 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 Axial length. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Axial length. This is the starting point the study compared everyone against.
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
Questions about rs9811920
What is rs9811920?
rs9811920 is a single position in the genome, in or near the FILIP1L gene. Published research associates it with axial length. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What do people read about alongside rs9811920?
Subjects that appear in the title or abstract of the same papers as this rsID include short-sightedness and screens (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs9811920 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 rs9811920 come from?
GWAS Catalog, Am J Hum Genet 2013, PMID:24144296. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
2 525217233128Reads by AI crawlersClaude5ChatGPT2Google · Gemini0Perplexity1Meta AI7Microsoft · Copilot2Amazon3Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others28Total52Counted 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
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