Sensitive

Venous thromboembolism

RBFOX1 · rs76668186

Where this position leads

Condition: Venous Thromboembolism

rs76668186 Condition: Venous Thromboembolism Venous Thromboembolism Condition rs76668186 rs76668186 RBFOX1

What the study found

Who was studied 7,482 African ancestry cases, 129,975 African ancestry controls.

The effect Each copy of the A allele shifted the measure 0.578 lower (95% confidence interval 0.37-0.78); p = 5 × 10−8.

How common The A allele had a frequency of about 96% in the people studied.

Where it sits Chromosome 16, band 16p13.3 — in an intron of RBFOX1.

What each result means

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

Questions about rs76668186

What is rs76668186?

rs76668186 is a single position in the genome, in or near the RBFOX1 gene. Published research associates it with venous thromboembolism. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs76668186 linked to?

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

Does having rs76668186 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 rs76668186 come from?

GWAS Catalog, Circulation 2022, PMID:36154123. 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.

Venous thromboembolism (rs76668186). MyGeneLog™. https://www.mygenelog.com/variants/rs76668186

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