Standard

Creatinine levels

DAB2 · rs10062079

Where this position leads

Condition: Kidney Function

rs10062079 Condition: Kidney Function Kidney Function Condition rs10062079 rs10062079 DAB2

What the study found

Who was studied 98,316 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.000815 higher (95% confidence interval 0.00062-0.00101); p = 3 × 10−17.

How common The A allele had a frequency of about 42% in the people studied.

Where it sits Chromosome 5, band 5p13.1 — in an intron of DAB2.

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 rs10062079

What is rs10062079?

rs10062079 is a single position in the genome, in or near the DAB2 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 rs10062079 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 rs10062079 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 rs10062079 come from?

GWAS Catalog, Ophthalmology science 2024, PMID:39091897. 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 (rs10062079). MyGeneLog™. https://www.mygenelog.com/variants/rs10062079

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