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Blood protein levels

near RPL31P44 · rs1194614

What the study found

Who was studied 3,200 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.289 lower (95% confidence interval 0.24-0.34); p = 1 × 10−31.

How common The T allele had a frequency of about 42% in the people studied.

Where it sits Chromosome 10, band 10q21.1 — between genes, 14.1 kb from RPL31P44.

What each result means

C/C No copy of the version the research linked to Blood protein levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Blood protein levels. That is a smaller link than two copies.
T/T 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.
Source

Questions about rs1194614

What is rs1194614?

rs1194614 is a single position in the genome, in or near the near RPL31P44 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 rs1194614 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 rs1194614 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 (rs1194614). MyGeneLog™. https://www.mygenelog.com/variants/rs1194614

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