2 5252315223326Reads by AI crawlersClaude5ChatGPT2Google · Gemini3Perplexity1Meta AI5Microsoft · Copilot2Amazon2Apple3China (ByteDance, Huawei, Baidu…)3ByteDance (Doubao)3Others26Total52Counted 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 0.122 higher (95% confidence interval 0.08-0.164); p = 1 × 10−8.
How common The A allele had a frequency of about 91% in the people studied.
Where it sits Chromosome 6, band 6q22.33 — in an intron of LOC102723409.
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 rs12193446
What is rs12193446?
rs12193446 is a single position in the genome, in or near the ARHGAP18 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 rs12193446?
Subjects that appear in the title or abstract of the same papers as this rsID include short-sightedness and screens (3 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs12193446 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 rs12193446 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 5252315223326Reads by AI crawlersClaude5ChatGPT2Google · Gemini3Perplexity1Meta AI5Microsoft · Copilot2Amazon2Apple3China (ByteDance, Huawei, Baidu…)3ByteDance (Doubao)3Others26Total52Counted 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.