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Plasma serine protease inhibitor levels

SERPINA5 · rs6119

What the study found

Who was studied 10,708 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.564 lower (95% confidence interval 0.52-0.61); p = 7 × 10−150.

How common The A allele had a frequency of about 90% in the people studied.

Where it sits Chromosome 14, band 14q32.13 — a missense change in SERPINA5.

What each result means

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

Questions about rs6119

What is rs6119?

rs6119 is a single position in the genome, in or near the SERPINA5 gene. Published research associates it with plasma serine protease inhibitor levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs6119 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 rs6119 come from?

GWAS Catalog, Science (New York, N.Y.) 2021, PMID:34648354. 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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Plasma serine protease inhibitor levels (rs6119). MyGeneLog™. https://www.mygenelog.com/variants/rs6119

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