Standard

Creatinine levels

DDIT4L-AS1 · rs28642089

Where this position leads

Condition: Kidney Function

rs28642089 Condition: Kidney Function Kidney Function Condition rs28642089 rs28642089 DDIT4L-AS1

What the study found

Who was studied 507,850 East Asian ancestry individuals, 420,829 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0103 lower (95% confidence interval 0.0078-0.0128); p = 2 × 10−16.

Where it sits Chromosome 4, band 4q24 — in an intron of DDIT4L-AS1.

What each result means

A/A Two copies of the version the research linked to Creatinine 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 Creatinine levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to Creatinine levels. This is the starting point the study compared everyone against.
Source

Questions about rs28642089

What is rs28642089?

rs28642089 is a single position in the genome, in or near the DDIT4L-AS1 gene. Published research associates it with creatinine 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 rs28642089 linked to?

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

Does having rs28642089 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 rs28642089 come from?

GWAS Catalog, Nature communications 2025, PMID:40436827. 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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Creatinine levels (rs28642089). MyGeneLog™. https://www.mygenelog.com/variants/rs28642089

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