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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 1,890 Korculan or Shetland Isles (founder/genetic isolate) individuals.
The effect
Each copy of the A allele shifted the measure 0.259 lower (95% confidence interval 0.18-0.34); p = 5 × 10−10.
How common The A allele had a frequency of about 21% in the people studied.
Where it sits Chromosome 2, band 2q21.2 — between genes, 17.2 kb from MGAT5.
What each result means
A/ATwo copies of the version the research linked to Transferrin N-glycan 27 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Transferrin N-glycan 27 levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Transferrin N-glycan 27 levels. This is the starting point the study compared everyone against.
Nature communications · 2022 · PMID 35332118 · open access
Questions about rs56157644
What is rs56157644?
rs56157644 is a single position in the genome, in or near the near MGAT5 gene. Published research associates it with transferrin n-glycan 27 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs56157644 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 rs56157644 come from?
GWAS Catalog, Nature communications 2022, PMID:35332118. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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