Sensitive

Coronary artery disease

PPAP2B · rs4634932

Where this position leads

Condition: Coronary Artery Disease

rs4634932 Condition: Coronary Artery Disease Coronary Artery Disease Condition rs4634932 rs4634932 PPAP2B

What the study found

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

The effect Each copy of the T allele shifted the measure 0.129 higher (95% confidence interval 0.1-0.15); p = 1 × 10−25.

How common The T allele had a frequency of about 92% in the people studied.

Where it sits Chromosome 1, band 1p32.2 — in an intron of PLPP3.

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 rs4634932

What is rs4634932?

rs4634932 is a single position in the genome, in or near the PPAP2B 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 rs4634932 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 rs4634932 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 rs4634932 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

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.

Coronary artery disease (rs4634932). MyGeneLog™. https://www.mygenelog.com/variants/rs4634932

← See all variants