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Brain N-acetylglucosaminylasparagine levels

AGA · rs1105059

What the study found

Who was studied 1,016 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0259 lower (95% confidence interval 0.019-0.033); p = 4 × 10−14.

Where it sits Chromosome 4, band 4q34.3 — in an intron of AGA.

What each result means

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

Questions about rs1105059

What is rs1105059?

rs1105059 is a single position in the genome, in or near the AGA gene. Published research associates it with brain n-acetylglucosaminylasparagine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs1105059 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 rs1105059 come from?

GWAS Catalog, Nature genetics 2024, PMID:39528826. 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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Brain N-acetylglucosaminylasparagine levels (rs1105059). MyGeneLog™. https://www.mygenelog.com/variants/rs1105059

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