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Appendicular lean mass

PLA2G3 · rs56195223

What the study found

Who was studied 450,243 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0247 lower (95% confidence interval 0.019-0.031); p = 4 × 10−16.

How common The T allele had a frequency of about 89% in the people studied.

Where it sits Chromosome 22, band 22q12.2 — between genes, 4.7 kb from PLA2G3.

What each result means

C/C No copy of the version the research linked to Appendicular lean mass. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Appendicular lean mass. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Appendicular lean mass. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs56195223

What is rs56195223?

rs56195223 is a single position in the genome, in or near the PLA2G3 gene. Published research associates it with appendicular lean mass. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs56195223 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 rs56195223 come from?

GWAS Catalog, Communications biology 2020, PMID:33097823. 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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Appendicular lean mass (rs56195223). MyGeneLog™. https://www.mygenelog.com/variants/rs56195223

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