Sensitive

Coronary artery disease

BMP1 · rs73225842

Where this position leads

Condition: Coronary Artery Disease

rs73225842 Condition: Coronary Artery Disease Coronary Artery Disease Condition rs73225842 rs73225842 BMP1

What the study found

Who was studied 34,541 cases, 261,984 controls; replicated in 88,192 cases, 162,544 controls.

The effect Each copy of the T allele shifted the measure 0.096 higher (95% confidence interval 0.067-0.125); p = 2 × 10−10.

How common The T allele had a frequency of about 5% in the people studied.

Where it sits Chromosome 8, band 8p21.3 — in an intron of BMP1.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Coronary artery disease — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Coronary artery disease.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Coronary artery disease compared to the general population.
Source

Questions about rs73225842

What is rs73225842?

rs73225842 is a single position in the genome, in or near the BMP1 gene. Published research associates it with coronary 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 rs73225842 linked to?

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

Does having rs73225842 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 rs73225842 come from?

GWAS Catalog, Circ Res 2017, PMID:29212778. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Coronary artery disease (rs73225842). MyGeneLog™. https://www.mygenelog.com/variants/rs73225842

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