Sensitive

Urinary metabolite levels in chronic kidney disease

RNPEP · rs56768485

What the study found

Who was studied 1,221 cases; replicated in 406 cases.

The effect Each copy of the A allele shifted the measure 0.355 higher (95% confidence interval 0.31-0.4); p = 1 × 10−56.

How common The A allele had a frequency of about 28% in the people studied.

Where it sits Chromosome 1, band 1q32.1 — in an intron of RNPEP.

What each result means

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

Questions about rs56768485

What is rs56768485?

rs56768485 is a single position in the genome, in or near the RNPEP gene. Published research associates it with urinary metabolite 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 rs56768485 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 rs56768485 come from?

GWAS Catalog, Nature genetics 2020, PMID:31959995. 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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Urinary metabolite levels in chronic kidney disease (rs56768485). MyGeneLog™. https://www.mygenelog.com/variants/rs56768485

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