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Triacylglycerol(56:5)_[M+NH4]1+ levels

PNPLA3 · rs13055900

What the study found

Who was studied 5,662 Pakistani ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0625 higher (95% confidence interval 0.051-0.074); p = 2 × 10−25.

Where it sits Chromosome 22, band 22q13.31 — in an intron of PNPLA3.

What each result means

A/A No copy of the version the research linked to Triacylglycerol(56:5)_[M+NH4]1+ levels. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Triacylglycerol(56:5)_[M+NH4]1+ levels. That is a smaller link than two copies.
G/G Two copies of the version the research linked to Triacylglycerol(56:5)_[M+NH4]1+ levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs13055900

What is rs13055900?

rs13055900 is a single position in the genome, in or near the PNPLA3 gene. Published research associates it with triacylglycerol(56:5)_[m+nh4]1+ levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs13055900 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 rs13055900 come from?

GWAS Catalog, BMC medicine 2021, PMID:34503513. 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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Triacylglycerol(56:5)_[M+NH4]1+ levels (rs13055900). MyGeneLog™. https://www.mygenelog.com/variants/rs13055900

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