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C-reactive protein levels

HNRNPC · rs11156891

Where this position leads

Condition: C-Reactive Protein Levels

rs11156891 Condition: C-Reactive Protein Levels C-Reactive Protein Levels Condition rs11156891 rs11156891 HNRNPC

What the study found

Who was studied 575,531 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0163 lower (95% confidence interval 0.011-0.021); p = 2 × 10−10.

Where it sits Chromosome 14, band 14q11.2 — in an intron of HNRNPC.

What each result means

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

Questions about rs11156891

What is rs11156891?

rs11156891 is a single position in the genome, in or near the HNRNPC gene. Published research associates it with c-reactive protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs11156891 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 rs11156891 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 rs11156891 come from?

GWAS Catalog, Nature communications 2022, PMID:35459240. 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 levels (rs11156891). MyGeneLog™. https://www.mygenelog.com/variants/rs11156891

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