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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 0.161 higher (95% confidence interval 0.11-0.21); p = 1 × 10−11.
Where it sits Chromosome 14, band 14q23.2 — inside SYNE2.
What each result means
A/ANo copy of the version the research linked to Sphingomyelin (d18:1/14:0) levels/Sphingomyelin (d16:1/16:0) levels. This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to Sphingomyelin (d18:1/14:0) levels/Sphingomyelin (d16:1/16:0) levels. That is a smaller link than two copies.
C/CTwo copies of the version the research linked to Sphingomyelin (d18:1/14:0) levels/Sphingomyelin (d16:1/16:0) 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 rs4591051
What is rs4591051?
rs4591051 is a single position in the genome, in or near the SYNE2 gene. Published research associates it with sphingomyelin (d18:1/14:0) levels/sphingomyelin (d16:1/16:0) levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs4591051 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 rs4591051 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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