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C-reactive protein

TIMM29 · rs113439314

Where this position leads

Condition: C-Reactive Protein Levels

rs113439314 Condition: C-Reactive Protein Levels C-Reactive Protein Levels Condition rs113439314 rs113439314 TIMM29

What the study found

Who was studied 353,466 European ancestry individuals, 83,025 East Asian ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.024 higher (95% confidence interval 0.016-0.032); p = 2 × 10−9.

Where it sits Chromosome 19, band 19p13.2 — inside TIMM29.

What each result means

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

Questions about rs113439314

What is rs113439314?

rs113439314 is a single position in the genome, in or near the TIMM29 gene. Published research associates it with c-reactive protein. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs113439314 linked to?

On MyGeneLog this position is linked to C-Reactive Protein Levels. The research behind each link, and its sources, are set out on that condition page.

Does having rs113439314 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 rs113439314 come from?

GWAS Catalog, Nature genetics 2021, PMID:34594039. 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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C-reactive protein (rs113439314). MyGeneLog™. https://www.mygenelog.com/variants/rs113439314

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