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3-Hydroxybutyrate levels

near SERPINA6 · rs145730801

What the study found

Who was studied 113,594 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0643 higher (95% confidence interval 0.044-0.084); p = 2 × 10−10.

How common The T allele had a frequency of about 96% in the people studied.

Where it sits Chromosome 14, band 14q32.13 — between genes, 2.4 kb from SERPINA6.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of 3-Hydroxybutyrate levels — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with 3-Hydroxybutyrate levels.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of 3-Hydroxybutyrate levels compared to the general population.
Source

Questions about rs145730801

What is rs145730801?

rs145730801 is a single position in the genome, in or near the near SERPINA6 gene. Published research associates it with 3-hydroxybutyrate levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs145730801 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 rs145730801 come from?

GWAS Catalog, PLoS biology 2022, PMID:35213538. 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.

3-Hydroxybutyrate levels (rs145730801). MyGeneLog™. https://www.mygenelog.com/variants/rs145730801

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