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Who was studied 9,689 Korean ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.351 g/dL lower; p = 2 × 10−35.
How common The G allele had a frequency of about 10% in the people studied.
Where it sits Chromosome 8, band 8p23.2 — in an intron of CSMD1.
What each result means
C/CNo copy of the version the research linked to Mean corpuscular hemoglobin concentration. This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Mean corpuscular hemoglobin concentration. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Mean corpuscular hemoglobin concentration. That is the strongest link of the three results. A link in a study is not a diagnosis.
Scientific reports · 2022 · PMID 35121771 · open access
Questions about rs73185547
What is rs73185547?
rs73185547 is a single position in the genome, in or near the CSMD1 gene. Published research associates it with mean corpuscular hemoglobin concentration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs73185547 linked to?
On MyGeneLog this position is linked to Blood Cell Counts. The research behind each link, and its sources, are set out on that condition page.
Does having rs73185547 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 rs73185547 come from?
GWAS Catalog, Scientific reports 2022, PMID:35121771. 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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Mean corpuscular hemoglobin concentration (rs73185547). MyGeneLog™. https://www.mygenelog.com/variants/rs73185547