Sensitive

Plasma X-24588 levels in chronic kidney disease

ABCC2 · rs55672373

What the study found

Who was studied 4,869 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.159 lower (95% confidence interval 0.11-0.21); p = 2 × 10−11.

How common The T allele had a frequency of about 5% in the people studied.

Where it sits Chromosome 10, band 10q24.2 — in an intron of ABCC2.

What each result means

C/C No copy of the version the research linked to Plasma X-24588 levels in chronic kidney disease. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Plasma X-24588 levels in chronic kidney disease. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Plasma X-24588 levels in chronic kidney disease. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs55672373

What is rs55672373?

rs55672373 is a single position in the genome, in or near the ABCC2 gene. Published research associates it with plasma x-24588 levels in chronic kidney disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs55672373 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 rs55672373 come from?

GWAS Catalog, Nature genetics 2023, PMID:37277652. 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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Plasma X-24588 levels in chronic kidney disease (rs55672373). MyGeneLog™. https://www.mygenelog.com/variants/rs55672373

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