Sensitive

Urinary metabolite levels in chronic kidney disease

TRIM48 · rs61898064

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 0.625 lower (95% confidence interval 0.56-0.69); p = 1 × 10−73.

How common The T allele had a frequency of about 5% in the people studied.

Where it sits Chromosome 11, band 11q11 — between genes, 197.3 kb from TRIM48.

What each result means

G/G 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.
G/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 rs61898064

What is rs61898064?

rs61898064 is a single position in the genome, in or near the TRIM48 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 rs61898064 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 rs61898064 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 (rs61898064). MyGeneLog™. https://www.mygenelog.com/variants/rs61898064

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