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Serum ceruloplasmin levels

CP · rs13072552

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What the study found

Who was studied 2,647 European ancestry individuals; replicated in 2,050 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 1.5 mg/dl higher (95% confidence interval -); p = 2 × 10⁻¹¹.

How common The T allele had a frequency of about 8% in the people studied.

Where it sits Chromosome 3, band 3q24 — in an intron of CP.

What each result means

G/G No copy of the version the research linked to Serum ceruloplasmin levels. This is the starting point the study compared everyone against.

G/T One copy of the version the research linked to Serum ceruloplasmin levels. That is a smaller link than two copies.

T/T Two copies of the version the research linked to Serum ceruloplasmin levels. That is the strongest link of the three results. A link in a study is not a diagnosis.

Source

Clinical and genetic association of serum ceruloplasmin with cardiovascular risk

Tang WH, Wu Y, Hartiala J, Fan Y, Stewart AF, Roberts R, McPherson R, Fox PL, Allayee H, Hazen SL

Arteriosclerosis, thrombosis, and vascular biology · 2012 · PMID 22075249

What people read about alongside this

Heart and circulation2

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs13072552

What is rs13072552?

rs13072552 is a single position in the genome, in or near the CP gene. Published research associates it with serum ceruloplasmin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What do people read about alongside rs13072552?

Subjects that appear in the title or abstract of the same papers as this rsID include heart and circulation (2 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs13072552 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 rs13072552 come from?

GWAS Catalog, Arterioscler Thromb Vasc Biol 2011, PMID:22075249. 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.

Serum ceruloplasmin levels (rs13072552). MyGeneLog™. https://www.mygenelog.com/variants/rs13072552

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