A/APublished research associates this genotype with typical/baseline likelihood of Parkinson's disease — no copies of the reported risk allele. (GWAS Catalog, Lancet 2011, PMID:21292315)
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Parkinson's disease. (GWAS Catalog, Lancet 2011, PMID:21292315)
G/GPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Parkinson's disease compared to the general population. (GWAS Catalog, Lancet 2011, PMID:21292315)
Source: GWAS Catalog, Lancet 2011, PMID:21292315
Questions about rs11711441
What is rs11711441?
rs11711441 is a single position in the genome, in or near the MCCC1 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 rs11711441 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.
Does having rs11711441 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 rs11711441 come from?
GWAS Catalog, Lancet 2011, PMID:21292315. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.