C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Polycystic ovary syndrome compared to the general population. (GWAS Catalog, Am J Obstet Gynecol 2020, PMID:32289280)
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Polycystic ovary syndrome. (GWAS Catalog, Am J Obstet Gynecol 2020, PMID:32289280)
T/TPublished research associates this genotype with typical/baseline likelihood of Polycystic ovary syndrome — no copies of the reported risk allele. (GWAS Catalog, Am J Obstet Gynecol 2020, PMID:32289280)
Source: GWAS Catalog, Am J Obstet Gynecol 2020, PMID:32289280
Questions about rs17186366
What is rs17186366?
rs17186366 is a single position in the genome, in or near the SOD2 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 rs17186366 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 rs17186366 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 rs17186366 come from?
GWAS Catalog, Am J Obstet Gynecol 2020, PMID:32289280. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.