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Heart failure with preserved ejection fraction

BRAP · rs11066001

Where this position leads

What the study found

Who was studied 7,154 Japanese ancestry cases, 197,577 Japanese ancestry controls; replicated in 19,589 European ancestry cases, 258,943 European ancestry controls.

The effect Each copy of the C allele shifted the measure 0.145 lower (95% confidence interval 0.1-0.19); p = 2 × 10⁻¹⁰.

How common The C allele had a frequency of about 25% in the people studied.

Where it sits Chromosome 12, band 12q24.12 — in an intron of BRAP.

What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Heart failure with preserved ejection fraction compared to the general population.

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Heart failure with preserved ejection fraction.

T/T Published research associates this genotype with typical/baseline likelihood of Heart failure with preserved ejection fraction — no copies of the reported risk allele.

Source

Genome-wide analysis of heart failure yields insights into disease heterogeneity and enables prognostic prediction in the Japanese population

Enzan N, Miyazawa K, Koyama S, Kurosawa R, Ieki H, Yoshida H, Takechi F, Fukuyama M, Osako R, Tomizuka K, Liu X, Ozaki K

and 18 more — show all

Onouchi Y, Matsuda K, Momozawa Y, Aburatani H, Kamatani Y, Yamaguchi T, Akazawa H, Node K, Ellinor PT, Levin MG, Damrauer SM, Voight BF, Joseph J, Sun YV, Terao C, Ninomiya T, Komuro I, Ito K

BioBank Japan Project

Nature communications · 2025 · PMID 41184235 · open access

Questions about rs11066001

What is rs11066001?

rs11066001 is a single position in the genome, in or near the BRAP gene. Published research associates it with heart failure with preserved ejection fraction. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs11066001 linked to?

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

Does having rs11066001 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 rs11066001 come from?

GWAS Catalog, Nature communications 2025, PMID:41184235. 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.

Heart failure with preserved ejection fraction (rs11066001). MyGeneLog™. https://www.mygenelog.com/variants/rs11066001

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