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Serum levels of protein CBR3

CBR3 · rs12483755

What the study found

Who was studied 5,363 Icelandic ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.657 lower (95% confidence interval 0.62-0.69); p = 6 × 10−286.

How common The A allele had a frequency of about 31% in the people studied.

Where it sits Chromosome 21, band 21q22.12 — in an intron of CBR3.

What each result means

A/A Two copies of the version the research linked to Serum levels of protein CBR3. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Serum levels of protein CBR3. That is a smaller link than two copies.
G/G No copy of the version the research linked to Serum levels of protein CBR3. This is the starting point the study compared everyone against.
Source

Questions about rs12483755

What is rs12483755?

rs12483755 is a single position in the genome, in or near the CBR3 gene. Published research associates it with serum levels of protein cbr3. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs12483755 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 rs12483755 come from?

GWAS Catalog, Nature communications 2022, PMID:35078996. 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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Serum levels of protein CBR3 (rs12483755). MyGeneLog™. https://www.mygenelog.com/variants/rs12483755

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