Sensitive

Plasma xanthurenate levels in chronic kidney disease

near SLC17A3 · rs473913

What the study found

Who was studied 4,741 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.127 higher (95% confidence interval 0.09-0.164); p = 8 × 10−12.

How common The T allele had a frequency of about 68% in the people studied.

Where it sits Chromosome 6, band 6p22.2 — between genes, 1.4 kb from SLC17A3.

What each result means

C/C No copy of the version the research linked to Plasma xanthurenate 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 Plasma xanthurenate levels in chronic kidney disease. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Plasma xanthurenate 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 rs473913

What is rs473913?

rs473913 is a single position in the genome, in or near the near SLC17A3 gene. Published research associates it with plasma xanthurenate 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 rs473913 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 rs473913 come from?

GWAS Catalog, GWAS Catalog n.d., 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 xanthurenate levels in chronic kidney disease (rs473913). MyGeneLog™. https://www.mygenelog.com/variants/rs473913

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