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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 22,730 European ancestry individuals.
The effect
The reported allele is G; the catalogue records no effect size
; p = 8 × 10−9.
Where it sits Chromosome 11, band 11q12.1 — in a non-coding transcript of OR5M7P.
What each result means
A/ANo copy of the version the research linked to Olfactory dysfunction. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Olfactory dysfunction. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Olfactory dysfunction. That is the strongest link of the three results. A link in a study is not a diagnosis.
BMC genomic data · 2025 · PMID 40963118 · open access
Questions about rs627933
What is rs627933?
rs627933 is a single position in the genome, in or near the near OR5M8 gene. Published research associates it with olfactory dysfunction. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs627933 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 rs627933 come from?
GWAS Catalog, BMC genomic data 2025, PMID:40963118. 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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