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Granzyme A (analyte X3440.7) levels

near CDC20B · rs13160656

What the study found

Who was studied 3,506 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.186 higher (95% confidence interval 0.13-0.24); p = 2 × 10−10.

How common The A allele had a frequency of about 21% in the people studied.

Where it sits Chromosome 5, band 5q11.2 — between genes, 22.5 kb from CDC20B.

What each result means

A/A Two copies of the version the research linked to Granzyme A (analyte X3440.7) levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Granzyme A (analyte X3440.7) levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to Granzyme A (analyte X3440.7) levels. This is the starting point the study compared everyone against.
Source

Questions about rs13160656

What is rs13160656?

rs13160656 is a single position in the genome, in or near the near CDC20B gene. Published research associates it with granzyme a (analyte x3440.7) levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs13160656 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 rs13160656 come from?

GWAS Catalog, Nature genetics 2024, PMID:39528825. 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.

Granzyme A (analyte X3440.7) levels (rs13160656). MyGeneLog™. https://www.mygenelog.com/variants/rs13160656

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