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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 31,120 Caucasian ancestry individuals.
The effect
Each copy of the G allele shifted the measure 17.6 (zscore) higher; p = 3 × 10−69.
How common The G allele had a frequency of about 51% in the people studied.
Where it sits Chromosome 19, band 19p13.2 — in an intron of CERS4.
What each result means
A/ANo copy of the version the research linked to Sphingomyeline C18:0 levels. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Sphingomyeline C18:0 levels. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Sphingomyeline C18:0 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs12610250 is a single position in the genome, in or near the CERS4 gene. Published research associates it with sphingomyeline c18:0 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs12610250 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 rs12610250 come from?
GWAS Catalog, Nature genetics 2021, PMID:33414548. 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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