Standard

Procalcitonin levels (adjusted for BMI)

CALCB · rs10832337

What the study found

Who was studied 12,448 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.031 higher (95% confidence interval 0.021-0.041); p = 5 × 10−9.

How common The A allele had a frequency of about 33% in the people studied.

Where it sits Chromosome 11, band 11p15.2 — inside CALCB.

What each result means

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

Questions about rs10832337

What is rs10832337?

rs10832337 is a single position in the genome, in or near the CALCB gene. Published research associates it with procalcitonin levels (adjusted for bmi). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10832337 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 rs10832337 come from?

GWAS Catalog, EBioMedicine 2026, PMID:41406505. 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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Procalcitonin levels (adjusted for BMI) (rs10832337). MyGeneLog™. https://www.mygenelog.com/variants/rs10832337

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