Sensitive

Urine X-24588 levels in chronic kidney disease

SLCO1B3-SLCO1B7 · rs4149128

What the study found

Who was studied 4,910 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.088 higher (95% confidence interval 0.063-0.113); p = 3 × 10−11.

How common The G allele had a frequency of about 82% in the people studied.

Where it sits Chromosome 12, band 12p12.2 — in an intron of SLCO1B3-SLCO1B7.

What each result means

C/C No copy of the version the research linked to Urine X-24588 levels in chronic kidney disease. This is the starting point the study compared everyone against.
C/G One copy of the version the research linked to Urine X-24588 levels in chronic kidney disease. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Urine X-24588 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 rs4149128

What is rs4149128?

rs4149128 is a single position in the genome, in or near the SLCO1B3-SLCO1B7 gene. Published research associates it with urine x-24588 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 rs4149128 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 rs4149128 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 X-24588 levels in chronic kidney disease (rs4149128). MyGeneLog™. https://www.mygenelog.com/variants/rs4149128

← See all variants