4 442225222225Reads by AI crawlersClaude2ChatGPT2Google · Gemini0Perplexity2Meta AI5Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others25Total44Counted 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.
Who was studied 1,713 European ancestry cases, 3,978 European ancestry controls; replicated in 3,361 European ancestry cases, 4,573 European ancestry controls.
The effect
Each copy of the A allele carried 1.30 times the odds of Parkinson's disease; p = 2 × 10−16.
How common The A allele had a frequency of about 82% in the people studied.
Where it sits Chromosome 17, band 17q21.31 — in an intron of LINC02210-CRHR1.
What each result means
A/ATwo copies of the version the research linked to Parkinson's disease. 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 Parkinson's disease. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Parkinson's disease. 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 rs393152
What is rs393152?
rs393152 is a single position in the genome, in or near the MAPT gene. Published research associates it with parkinson's disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs393152 linked to?
On MyGeneLog this position is linked to Parkinson's Disease. The research behind each link, and its sources, are set out on that condition page.
What do people read about alongside rs393152?
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 rs393152 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 rs393152 come from?
GWAS Catalog, Nat Genet 2009, PMID:19915575. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
4 442225222225Reads by AI crawlersClaude2ChatGPT2Google · Gemini0Perplexity2Meta AI5Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others25Total44Counted 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.
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