C/CPublished research associates this genotype with typical/baseline likelihood of Schizophrenia — no copies of the reported risk allele.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Schizophrenia.
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Schizophrenia compared to the general population.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2015 · PMID 26198764
Questions about rs1367858
What is rs1367858?
rs1367858 is a single position in the genome, in or near the near SPATS2L 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 rs1367858 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 rs1367858 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 rs1367858 come from?
GWAS Catalog, Am J Med Genet B Neuropsychiatr Genet 2015, PMID:26198764. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.