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Blood protein levels

APMAP · rs2150649

What the study found

Who was studied 3,200 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.43 higher (95% confidence interval 0.34-0.52); p = 2 × 10−19.

How common The C allele had a frequency of about 93% in the people studied.

Where it sits Chromosome 20, band 20p11.21 — between genes, 75.8 kb from LINC02967.

What each result means

C/C 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.
C/T One copy of the version the research linked to Blood protein levels. That is a smaller link than two copies.
T/T 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 rs2150649

What is rs2150649?

rs2150649 is a single position in the genome, in or near the APMAP 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 rs2150649 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 rs2150649 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 (rs2150649). MyGeneLog™. https://www.mygenelog.com/variants/rs2150649

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