Sensitive

Schizophrenia

NDST3 · rs11098403

Where this position leads

Condition: Schizophrenia

rs11098403 Condition: Schizophrenia Schizophrenia Condition rs11098403 rs11098403 NDST3

What the study found

Who was studied 904 Ashkenazi Jewish cases, 1,640 Ashkenazi Jewish controls; replicated in 3,944 European ancestry cases, 3,049 European ancestry controls, 921 African American cases, 954 African American controls, 550 Japanese ancestry cases, 530 Japanese ancestry controls.

The effect Each copy of the G allele carried 1.15 times the odds of Schizophrenia (95% confidence interval 1.08-1.21); p = 3 × 10−8.

Where it sits Chromosome 4, band 4q26 — between genes, 34.6 kb from LINC01378.

What each result means

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

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 rs11098403

What is rs11098403?

rs11098403 is a single position in the genome, in or near the NDST3 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 rs11098403 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 rs11098403?

Subjects that appear in the title or abstract of the same papers as this rsID include depression and stress (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs11098403 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 rs11098403 come from?

GWAS Catalog, Nat Commun 2013, PMID:24253340. 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 (rs11098403). MyGeneLog™. https://www.mygenelog.com/variants/rs11098403

← See all variants