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Serum urate levels

near LINC00970 · rs1892093

What the study found

Who was studied 630,117 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0228 higher (95% confidence interval 0.016-0.03); p = 2 × 10−10.

How common The T allele had a frequency of about 88% in the people studied.

Where it sits Chromosome 1, band 1q24.2 — between genes, 0.8 kb from LINC00970.

What each result means

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

Questions about rs1892093

What is rs1892093?

rs1892093 is a single position in the genome, in or near the near LINC00970 gene. Published research associates it with serum urate levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs1892093 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 rs1892093 come from?

GWAS Catalog, Nature genetics 2024, PMID:39406924. 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.

Serum urate levels (rs1892093). MyGeneLog™. https://www.mygenelog.com/variants/rs1892093

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