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Creatinine-cystatin C ratio

CUX2 · rs4766453

What the study found

Who was studied 274,251 British ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.335 higher (95% confidence interval 0.26-0.41); p = 1 × 10−17.

Where it sits Chromosome 12, band 12q24.11 — in an intron of CUX2.

What each result means

C/C No copy of the version the research linked to Creatinine-cystatin C ratio. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Creatinine-cystatin C ratio. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Creatinine-cystatin C ratio. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs4766453

What is rs4766453?

rs4766453 is a single position in the genome, in or near the CUX2 gene. Published research associates it with creatinine-cystatin c ratio. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs4766453 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 rs4766453 come from?

GWAS Catalog, Frontiers in endocrinology 2024, PMID:38836225. 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-cystatin C ratio (rs4766453). MyGeneLog™. https://www.mygenelog.com/variants/rs4766453

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