A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Schizophrenia compared to the general population. (GWAS Catalog, Nat Genet 2017, PMID:28991256)
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Schizophrenia. (GWAS Catalog, Nat Genet 2017, PMID:28991256)
G/GPublished research associates this genotype with typical/baseline likelihood of Schizophrenia — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2017, PMID:28991256)
rs2073499 is a single position in the genome, in or near the HYAL3 gene. Published research associates it with schizophrenia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs2073499 linked to?
On MyGeneLog this position is linked to Schizophrenia. The research behind each link, and its sources, are set out on that condition page.
Does having rs2073499 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 rs2073499 come from?
GWAS Catalog, Nat Genet 2017, PMID:28991256. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.