Standard

Serum protein levels (sST2)

IL1RL2 · rs2302612

Where this position leads

Condition: Serum sST2 Levels

rs2302612 Condition: Serum sST2 Levels Serum sST2 Levels Condition rs2302612 rs2302612 IL1RL2

What the study found

Who was studied 2,797 individuals.

The effect Each copy of the C allele shifted the measure 0.08 lower (95% confidence interval 0.06-0.1); p = 2 × 10−11.

How common The C allele had a frequency of about 17% in the people studied.

Where it sits Chromosome 2, band 2q12.1 — a missense change in IL1RL2.

What each result means

C/C Two copies of the version the research linked to Serum protein levels (sST2). 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 Serum protein levels (sST2). That is a smaller link than two copies.
T/T No copy of the version the research linked to Serum protein levels (sST2). This is the starting point the study compared everyone against.
Source

Questions about rs2302612

What is rs2302612?

rs2302612 is a single position in the genome, in or near the IL1RL2 gene. Published research associates it with serum protein levels (sst2). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs2302612 linked to?

On MyGeneLog this position is linked to Serum sST2 Levels. The research behind each link, and its sources, are set out on that condition page.

Does having rs2302612 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 rs2302612 come from?

GWAS Catalog, J Clin Invest 2013, PMID:23999434. 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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Serum protein levels (sST2) (rs2302612). MyGeneLog™. https://www.mygenelog.com/variants/rs2302612

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