1 462216123227Reads by AI crawlersClaude2ChatGPT2Google · Gemini0Perplexity1Meta AI6Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others27Total46Counted 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 13,708 European ancestry cases, 95,282 European ancestry controls; replicated in 5,353 European ancestry cases, 5,551 European ancestry controls.
The effect
Each copy of the T allele carried 1.13 times the odds of Parkinson's disease (95% confidence interval 1.09-1.17); p = 5 × 10−10.
How common The T allele had a frequency of about 14% in the people studied.
Where it sits Chromosome 1, band 1q42.2 — in an intron of SIPA1L2.
What each result means
C/CNo copy of the version the research linked to Parkinson's disease. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Parkinson's disease. That is a smaller link than two copies.
T/TTwo 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.
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 rs10797576
What is rs10797576?
rs10797576 is a single position in the genome, in or near the SIPA1L2 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 rs10797576 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 rs10797576?
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 rs10797576 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 rs10797576 come from?
GWAS Catalog, Nat Genet 2014, PMID:25064009. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
1 462216123227Reads by AI crawlersClaude2ChatGPT2Google · Gemini0Perplexity1Meta AI6Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others27Total46Counted 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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