A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Polycystic ovary syndrome compared to the general population.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Polycystic ovary syndrome.
G/GPublished research associates this genotype with typical/baseline likelihood of Polycystic ovary syndrome — no copies of the reported risk allele.
rs6022786 is a single position in the genome, in or near the SUMO1P1 gene. Published research associates it with polycystic ovary syndrome. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs6022786 linked to?
On MyGeneLog this position is linked to Polycystic Ovary Syndrome. The research behind each link, and its sources, are set out on that condition page.
Does having rs6022786 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 rs6022786 come from?
GWAS Catalog, Nat Genet 2012, PMID:22885925. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.