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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 38,932 British ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.095 higher (95% confidence interval 0.07-0.12); p = 7 × 10−14.
How common The A allele had a frequency of about 7% in the people studied.
Where it sits Chromosome 5, band 5q14.3 — in an intron of MIR9-2HG.
What each result means
A/ATwo copies of the version the research linked to Retinal vascular fractal dimension. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/TOne copy of the version the research linked to Retinal vascular fractal dimension. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Retinal vascular fractal dimension. This is the starting point the study compared everyone against.
rs75048985 is a single position in the genome, in or near the MIR9-2HG gene. Published research associates it with retinal vascular fractal dimension. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs75048985 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 rs75048985 come from?
GWAS Catalog, Circulation 2022, PMID:34743558. 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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