A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Parkinson's disease compared to the general population.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Parkinson's disease.
G/GPublished research associates this genotype with typical/baseline likelihood of Parkinson's disease — no copies of the reported risk allele.
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 rs11060180
What is rs11060180?
rs11060180 is a single position in the genome, in or near the CCDC62 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 rs11060180 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 rs11060180?
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 rs11060180 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 rs11060180 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.