4 482217123228Reads by AI crawlersClaude2ChatGPT2Google · Gemini0Perplexity1Meta AI7Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others28Total48Counted 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 2,020 European ancestry neuropsychiatric disorder cases, 5,775 European ancestry controls; replicated in 599 European ancestry neuropsychiatric disorder cases, 11,915 European ancestry controls, 143 European ancestry and African American neuropsychiatric disorder cases, 94 European ancestry and African American controls, 605 Hispanic controls.
The effect
Each copy of the C allele shifted the measure 9.01e+03 mm3 higher (95% confidence interval 6525.78-11487.64); p = 1 × 10−12.
How common The C allele had a frequency of about 49% in the people studied.
Where it sits Chromosome 12, band 12q14.3 — in an intron of HMGA2.
What each result means
C/CTwo copies of the version the research linked to Brain structure. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Brain structure. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Brain structure. 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 rs10784502
What is rs10784502?
rs10784502 is a single position in the genome, in or near the HMGA2 gene. Published research associates it with brain structure. 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 rs10784502?
Subjects that appear in the title or abstract of the same papers as this rsID include brain and memory (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 rs10784502 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 rs10784502 come from?
GWAS Catalog, Nat Genet 2012, PMID:22504417. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
4 482217123228Reads by AI crawlersClaude2ChatGPT2Google · Gemini0Perplexity1Meta AI7Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others28Total48Counted 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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