Sensitive

Urine N-lactoyl leucine levels in chronic kidney disease

DPEP1 · rs2460451

What the study found

Who was studied 4,890 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.352 lower (95% confidence interval 0.32-0.38); p = 2 × 10−110.

How common The A allele had a frequency of about 45% in the people studied.

Where it sits Chromosome 16, band 16q24.3 — in an intron of DPEP1.

What each result means

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

Questions about rs2460451

What is rs2460451?

rs2460451 is a single position in the genome, in or near the DPEP1 gene. Published research associates it with urine n-lactoyl leucine 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 rs2460451 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 rs2460451 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

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Urine N-lactoyl leucine levels in chronic kidney disease (rs2460451). MyGeneLog™. https://www.mygenelog.com/variants/rs2460451

← See all variants