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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 12,502 Hispanic/Latino individuals; replicated in 4,772 Hispanic/Latino individuals.
The effect
Each copy of the G allele shifted the measure 0.29 pg higher (95% confidence interval 0.19-0.39); p = 1 × 10−8.
How common The G allele had a frequency of about 92% in the people studied.
Where it sits Chromosome 6, band 6p21.1 — in an intron of CCND3.
What each result means
C/CNo copy of the version the research linked to Mean corpuscular hemoglobin. This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Mean corpuscular hemoglobin. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Mean corpuscular hemoglobin. That is the strongest link of the three results. A link in a study is not a diagnosis.
PLoS genetics · 2017 · PMID 28453575 · open access
Questions about rs9367125
What is rs9367125?
rs9367125 is a single position in the genome, in or near the CCND3 gene. Published research associates it with mean corpuscular hemoglobin. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs9367125 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 rs9367125 come from?
GWAS Catalog, PLoS genetics 2017, PMID:28453575. 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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Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Mean corpuscular hemoglobin (rs9367125). MyGeneLog™. https://www.mygenelog.com/variants/rs9367125