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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 45,330 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.13 higher (95% confidence interval 0.11-0.15); p = 8 × 10−33.
How common The T allele had a frequency of about 90% in the people studied.
Where it sits Chromosome 6, band 6p22.2 — between genes, 5.6 kb from TRIM38.
What each result means
C/CNo copy of the version the research linked to Soluble transferrin receptor concentration. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Soluble transferrin receptor concentration. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Soluble transferrin receptor concentration. That is the strongest link of the three results. A link in a study is not a diagnosis.
Communications biology · 2024 · PMID 39643614 · open access
Questions about rs72832593
What is rs72832593?
rs72832593 is a single position in the genome, in or near the near TRIM38 gene. Published research associates it with soluble transferrin receptor concentration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs72832593 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 rs72832593 come from?
GWAS Catalog, Communications biology 2024, PMID:39643614. 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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