Sensitive

Schizophrenia

MINDY2 · rs793571

Where this position leads

Condition: Autism Spectrum Disorder and Schizophrenia (Shared Genetic Risk)

rs793571 Condition: Autism Spectrum Disorder and Schizophrenia (Shared Genetic Risk) Autism Spectrum Disorder and Schizo… Condition rs793571 rs793571 MINDY2

What the study found

Who was studied 11,361 European ancestry female cases, 18,119 European ancestry female controls, 20,206 European ancestry male cases, 19,375 European ancestry male controls.

The effect Each copy of the A allele shifted the measure 0.129 higher (95% confidence interval 0.087-0.171); p = 1 × 10−9.

How common The A allele had a frequency of about 77% in the people studied.

Where it sits Chromosome 15, band 15q22.1 — in an intron of MINDY2.

What each result means

A/A Two copies of the version the research linked to 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 Schizophrenia. That is a smaller link than two copies.
G/G No copy of the version the research linked to Schizophrenia. This is the starting point the study compared everyone against.
Source

Questions about rs793571

What is rs793571?

rs793571 is a single position in the genome, in or near the MINDY2 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 rs793571 linked to?

On MyGeneLog this position is linked to Autism Spectrum Disorder and Schizophrenia (Shared Genetic Risk). The research behind each link, and its sources, are set out on that condition page.

Does having rs793571 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 rs793571 come from?

GWAS Catalog, Biological psychiatry 2022, PMID:34099189. 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.

Schizophrenia (rs793571). MyGeneLog™. https://www.mygenelog.com/variants/rs793571

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