Sensitive

Plasma X-24947 levels in chronic kidney disease

near UGT2B11 · rs114488830

What the study found

Who was studied 4,615 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.427 lower (95% confidence interval 0.33-0.52); p = 8 × 10−19.

How common The A allele had a frequency of about 8% in the people studied.

Where it sits Chromosome 4, band 4q13.2 — between genes, 9.5 kb from UGT2B11.

What each result means

A/A Two copies of the version the research linked to Plasma X-24947 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 Plasma X-24947 levels in chronic kidney disease. That is a smaller link than two copies.
G/G No copy of the version the research linked to Plasma X-24947 levels in chronic kidney disease. This is the starting point the study compared everyone against.
Source

Questions about rs114488830

What is rs114488830?

rs114488830 is a single position in the genome, in or near the near UGT2B11 gene. Published research associates it with plasma x-24947 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 rs114488830 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 rs114488830 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.

Plasma X-24947 levels in chronic kidney disease (rs114488830). MyGeneLog™. https://www.mygenelog.com/variants/rs114488830

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