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C-reactive protein levels

AFF4 · rs72799498

Where this position leads

Condition: C-Reactive Protein Levels

rs72799498 Condition: C-Reactive Protein Levels C-Reactive Protein Levels Condition rs72799498 rs72799498 AFF4

What the study found

Who was studied 575,531 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0166 higher (95% confidence interval 0.011-0.022); p = 2 × 10−9.

Where it sits Chromosome 5, band 5q31.1 — in an intron of AFF4.

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/G One copy of the version the research linked to C-reactive protein levels. That is a smaller link than two copies.
G/G 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 rs72799498

What is rs72799498?

rs72799498 is a single position in the genome, in or near the AFF4 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 rs72799498 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 rs72799498 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 rs72799498 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 (rs72799498). MyGeneLog™. https://www.mygenelog.com/variants/rs72799498

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