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Total bilirubin levels

USP40 · rs62192762

What the study found

Who was studied 341,077 European ancestry individuals, 5,978 African ancestry individuals, 7,313 South Asian ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.201 lower (95% confidence interval 0.19-0.21); p = 1 × 10−238.

Where it sits Chromosome 2, band 2q37.1 — in an intron of USP40.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Total bilirubin levels compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Total bilirubin levels.
G/G Published research associates this genotype with typical/baseline likelihood of Total bilirubin levels — no copies of the reported risk allele.
Source

Questions about rs62192762

What is rs62192762?

rs62192762 is a single position in the genome, in or near the USP40 gene. Published research associates it with total bilirubin levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs62192762 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 rs62192762 come from?

GWAS Catalog, Nature genetics 2021, PMID:33462484. 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.

Total bilirubin levels (rs62192762). MyGeneLog™. https://www.mygenelog.com/variants/rs62192762

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