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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 412,277 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.0347 lower (95% confidence interval 0.03-0.04); p = 9 × 10−40.
How common The A allele had a frequency of about 61% in the people studied.
Where it sits Chromosome 11, band 11p15.1 — in an intron of SERGEF.
What each result means
A/ATwo copies of the version the research linked to Bicarbonate (maximum, inv-norm transformed). 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 Bicarbonate (maximum, inv-norm transformed). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Bicarbonate (maximum, inv-norm transformed). This is the starting point the study compared everyone against.
Science (New York, N.Y.) · 2024 · PMID 39024449 · open access
Questions about rs2237908
What is rs2237908?
rs2237908 is a single position in the genome, in or near the SERGEF gene. Published research associates it with bicarbonate (maximum, inv-norm transformed). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2237908 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 rs2237908 come from?
GWAS Catalog, Science (New York, N.Y.) 2024, PMID:39024449. 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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