Sensitive

Peripheral artery disease

CREB3L1 · rs7476

Where this position leads

Condition: Peripheral Artery Disease

rs7476 Condition: Peripheral Artery Disease Peripheral Artery Disease Condition rs7476 rs7476 CREB3L1

What the study found

Who was studied 24,009 European ancestry cases, 150,983 European ancestry controls, 5,373 African ancestry cases, 42,485 African ancestry controls, 1,925 Hispanic cases, 18,285 Hispanic controls; replicated in 5,117 European ancestry cases, 389,291 European ancestry controls.

The effect Each copy of the C allele carried 1.06 times the odds of Peripheral artery disease (95% confidence interval 1.04-1.08); p = 8 × 10−10.

How common The C allele had a frequency of about 38% in the people studied.

Where it sits Chromosome 11, band 11p11.2 — in the 3′ untranslated region of CREB3L1.

What each result means

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

Questions about rs7476

What is rs7476?

rs7476 is a single position in the genome, in or near the CREB3L1 gene. Published research associates it with peripheral artery disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs7476 linked to?

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

Does having rs7476 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 rs7476 come from?

GWAS Catalog, Nature medicine 2019, PMID:31285632. 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.

Peripheral artery disease (rs7476). MyGeneLog™. https://www.mygenelog.com/variants/rs7476

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