Sensitive

Bipolar disorder

STK4 · rs6130764

Where this position leads

Condition: Bipolar Disorder

rs6130764 Condition: Bipolar Disorder Bipolar Disorder Condition rs6130764 rs6130764 STK4

What the study found

Who was studied 1,822 Han Chinese ancestry cases, 4,650 Han Chinese ancestry controls, 20,352 European ancestry cases, 31,358 European ancestry controls.

The effect Each copy of the T allele carried 1.07 times the odds of Bipolar disorder (95% confidence interval 1.044-1.091); p = 6 × 10−9.

Where it sits Chromosome 20, band 20q13.12 — between genes, 1.7 kb from WFDC12.

What each result means

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

Questions about rs6130764

What is rs6130764?

rs6130764 is a single position in the genome, in or near the STK4 gene. Published research associates it with bipolar disorder. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs6130764 linked to?

On MyGeneLog this position is linked to Bipolar Disorder. The research behind each link, and its sources, are set out on that condition page.

Does having rs6130764 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 rs6130764 come from?

GWAS Catalog, JAMA psychiatry 2021, PMID:33263727. 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.

Bipolar disorder (rs6130764). MyGeneLog™. https://www.mygenelog.com/variants/rs6130764

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