Sensitive

Schizophrenia

TRANK1 · rs75968099

Where this position leads

Condition: Schizophrenia

rs75968099 Condition: Schizophrenia Schizophrenia Condition rs75968099 rs75968099 TRANK1

What the study found

Who was studied 32,405 European ancestry cases, 42,221 European ancestry controls, 1,235 European ancestry cases and 1,235 European ancestry controls from 1235 parent-offspring trios, 1,836 East Asian ancestry cases, 3,383 East Asian ancestry controls; replicated in 1,513 European ancestry cases, 66,236 European ancestry controls.

The effect Each copy of the T allele carried 1.08 times the odds of Schizophrenia (95% confidence interval 1.062-1.109); p = 1 × 10−13.

How common The T allele had a frequency of about 32% in the people studied.

Where it sits Chromosome 3, band 3p22.2 — between genes, 2.2 kb from LINC02033.

What each result means

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

Questions about rs75968099

What is rs75968099?

rs75968099 is a single position in the genome, in or near the TRANK1 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 rs75968099 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 rs75968099 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 rs75968099 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.

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 (rs75968099). MyGeneLog™. https://www.mygenelog.com/variants/rs75968099

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