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Blood protein levels

CCDC126 · rs143669862

What the study found

Who was studied 3,200 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.261 lower (95% confidence interval 0.2-0.32); p = 4 × 10−19.

How common The A allele had a frequency of about 76% in the people studied.

Where it sits Chromosome 7, band 7p15.3 — in an intron of CCDC126.

What each result means

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

Questions about rs143669862

What is rs143669862?

rs143669862 is a single position in the genome, in or near the CCDC126 gene. Published research associates it with blood protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs143669862 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 rs143669862 come from?

GWAS Catalog, Science (New York, N.Y.) 2018, PMID:30072576. 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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Blood protein levels (rs143669862). MyGeneLog™. https://www.mygenelog.com/variants/rs143669862

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