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TPSAB1 protein levels

near PRSS29P · rs182106504

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.354 lower (95% confidence interval 0.25-0.45); p = 4 × 10−15.

How common The A allele had a frequency of about 0% in the people studied.

Where it sits Chromosome 16, band 16p13.3 — between genes, 10.5 kb from PRSS29P.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of TPSAB1 protein 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 TPSAB1 protein levels.
G/G Published research associates this genotype with typical/baseline likelihood of TPSAB1 protein levels — no copies of the reported risk allele.
Source

Questions about rs182106504

What is rs182106504?

rs182106504 is a single position in the genome, in or near the near PRSS29P gene. Published research associates it with tpsab1 protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs182106504 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 rs182106504 come from?

GWAS Catalog, Nature genetics 2025, PMID:39789286. 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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TPSAB1 protein levels (rs182106504). MyGeneLog™. https://www.mygenelog.com/variants/rs182106504

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