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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 4,492 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.195 higher (95% confidence interval 0.15-0.24); p = 4 × 10−15.
Where it sits Chromosome 22, band 22q13.2 — in an intron of A4GALT.
What each result means
A/ANo copy of the version the research linked to Dihexosylceramide (d18:1/24:0) levels. This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to Dihexosylceramide (d18:1/24:0) levels. That is a smaller link than two copies.
C/CTwo copies of the version the research linked to Dihexosylceramide (d18:1/24:0) levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2022 · PMID 35668104 · open access
Questions about rs13056962
What is rs13056962?
rs13056962 is a single position in the genome, in or near the A4GALT gene. Published research associates it with dihexosylceramide (d18:1/24:0) levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs13056962 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 rs13056962 come from?
GWAS Catalog, Nature communications 2022, PMID:35668104. 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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