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Urinary albumin-to-creatinine ratio

SBF2 · rs113139575

What the study found

Who was studied 547,361 European ancestry individuals, 6,795 African American individuals, 6,324 East Asian ancestry individuals, 2,335 South Asian ancestry individuals, 1,442 Hispanic individuals.

The effect Each copy of the C allele shifted the measure 0.025 lower (95% confidence interval 0.017-0.033); p = 6 × 10−10.

Where it sits Chromosome 11, band 11p15.4 — in an intron of SBF2.

What each result means

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

Questions about rs113139575

What is rs113139575?

rs113139575 is a single position in the genome, in or near the SBF2 gene. Published research associates it with urinary albumin-to-creatinine ratio. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs113139575 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 rs113139575 come from?

GWAS Catalog, Nature communications 2019, PMID:31511532. 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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Urinary albumin-to-creatinine ratio (rs113139575). MyGeneLog™. https://www.mygenelog.com/variants/rs113139575

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