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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 20,016 European ancestry cases, 380,433 European ancestry controls.
The effect
The reported allele is G; the catalogue records no effect size
; p = 3 × 10−9.
How common The G allele had a frequency of about 10% in the people studied.
Where it sits Chromosome 20, band 20q13.2 — between genes, 5 kb from CYP24A1.
What each result means
A/ANo copy of the version the research linked to Eczema. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Eczema. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Eczema. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2021 · PMID 34785669 · open access
Questions about rs73285914
What is rs73285914?
rs73285914 is a single position in the genome, in or near the near CYP24A1 gene. Published research associates it with eczema. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs73285914 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 rs73285914 come from?
GWAS Catalog, Nature communications 2021, PMID:34785669. 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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