Sensitive

Autism spectrum disorder or schizophrenia

HLA-DRB1 · rs184153866

Where this position leads

Condition: Schizophrenia

rs184153866 Condition: Schizophrenia Schizophrenia Condition rs184153866 rs184153866 HLA-DRB1

What the study found

Who was studied schizophrenia cases and controls (see Ripke, 2014), up to 6,197 European ancestry ASD cases, up to 7,377 European ancestry controls, up to 1,190 ASD cases, up to 1,190 controls.

The effect Each copy of the A allele carried 1.10 times the odds of Autism spectrum disorder or schizophrenia (95% confidence interval 1.08-1.13); p = 2 × 10−13.

Where it sits Chromosome 6, band 6p21.32 — between genes, 2.8 kb from HLA-DRB5.

What each result means

A/A Two copies of the version the research linked to Autism spectrum disorder or schizophrenia. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Autism spectrum disorder or schizophrenia. That is a smaller link than two copies.
G/G No copy of the version the research linked to Autism spectrum disorder or schizophrenia. This is the starting point the study compared everyone against.
Source

Questions about rs184153866

What is rs184153866?

rs184153866 is a single position in the genome, in or near the HLA-DRB1 gene. Published research associates it with autism spectrum disorder or 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 rs184153866 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 rs184153866 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 rs184153866 come from?

GWAS Catalog, Molecular autism 2017, PMID:28540026. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Autism spectrum disorder or schizophrenia (rs184153866). MyGeneLog™. https://www.mygenelog.com/variants/rs184153866

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