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Tryptase beta-2 levels

near TPSD1 · rs7199049

What the study found

Who was studied 2,935 Qatari ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.537 lower (95% confidence interval 0.4-0.67); p = 4 × 10−15.

How common The G allele had a frequency of about 4% in the people studied.

Where it sits Chromosome 16, band 16p13.3 — between genes, 0.9 kb from TPSD1.

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Tryptase beta-2 levels — no copies of the reported risk allele.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Tryptase beta-2 levels.
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Tryptase beta-2 levels compared to the general population.
Source

Questions about rs7199049

What is rs7199049?

rs7199049 is a single position in the genome, in or near the near TPSD1 gene. Published research associates it with tryptase beta-2 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs7199049 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 rs7199049 come from?

GWAS Catalog, Human molecular genetics 2023, PMID:36168886. 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.

Tryptase beta-2 levels (rs7199049). MyGeneLog™. https://www.mygenelog.com/variants/rs7199049

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