Sensitive

Schizophrenia

RIMS1 · rs1339227

Where this position leads

Condition: Schizophrenia

rs1339227 Condition: Schizophrenia Schizophrenia Condition rs1339227 rs1339227 RIMS1

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Schizophrenia compared to the general population. (GWAS Catalog, Nature 2014, PMID:25056061)
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Schizophrenia. (GWAS Catalog, Nature 2014, PMID:25056061)
T/T Published research associates this genotype with typical/baseline likelihood of Schizophrenia — no copies of the reported risk allele. (GWAS Catalog, Nature 2014, PMID:25056061)

Source: GWAS Catalog, Nature 2014, PMID:25056061

What people read about alongside this

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs1339227

What is rs1339227?

rs1339227 is a single position in the genome, in or near the RIMS1 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 rs1339227 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.

What do people read about alongside rs1339227?

Subjects that appear in the title or abstract of the same papers as this rsID include anxiety and worry (2 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs1339227 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 rs1339227 come from?

GWAS Catalog, Nature 2014, PMID:25056061. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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