Sensitive

Schizophrenia

LOC10050743 · rs10791098

Where this position leads

Condition: Schizophrenia

rs10791098 Condition: Schizophrenia Schizophrenia Condition rs10791098 rs10791098 LOC10050743

What the study found

Who was studied 14,023 East Asian ancestry cases, 33,640 European ancestry cases, 31,505 East Asian ancestry controls, 43,456 European ancestry controls.

The effect Each copy of the T allele carried 1.08 times the odds of Schizophrenia (95% confidence interval 1.06-1.1); p = 2 × 10−12.

Where it sits Chromosome 11, band 11q24.3 — in an intron of LINC02551.

What each result means

G/G No copy of the version the research linked to Schizophrenia. This is the starting point the study compared everyone against.
G/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 rs10791098

What is rs10791098?

rs10791098 is a single position in the genome, in or near the LOC10050743 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 rs10791098 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 rs10791098 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 rs10791098 come from?

GWAS Catalog, Schizophr Bull 2018, PMID:30285260. 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 (rs10791098). MyGeneLog™. https://www.mygenelog.com/variants/rs10791098

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