Sensitive

Urinary metabolite levels in chronic kidney disease

CYP4B1 · rs3863632

What the study found

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

The effect Each copy of the T allele shifted the measure 0.388 higher (95% confidence interval 0.29-0.49); p = 4 × 10−14.

How common The T allele had a frequency of about 12% in the people studied.

Where it sits Chromosome 1, band 1p33 — in an intron of CYP4Z2P.

What each result means

C/C 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.
C/T One copy of the version the research linked to Urinary metabolite levels in chronic kidney disease. That is a smaller link than two copies.
T/T 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.
Source

Questions about rs3863632

What is rs3863632?

rs3863632 is a single position in the genome, in or near the CYP4B1 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 rs3863632 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 rs3863632 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

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.

Urinary metabolite levels in chronic kidney disease (rs3863632). MyGeneLog™. https://www.mygenelog.com/variants/rs3863632

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