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Blood protein levels

BCAM · rs186872766

What the study found

Who was studied 3,200 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 1.02 lower (95% confidence interval 0.74-1.3); p = 1 × 10−12.

How common The G allele had a frequency of about 99% in the people studied.

Where it sits Chromosome 19, band 19q13.32 — in an intron of CBLC.

What each result means

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

Questions about rs186872766

What is rs186872766?

rs186872766 is a single position in the genome, in or near the BCAM 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 rs186872766 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 rs186872766 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 (rs186872766). MyGeneLog™. https://www.mygenelog.com/variants/rs186872766

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