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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 340,567 European ancestry individuals, 5,974 African ancestry individuals, 7,283 South Asian ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.0237 higher (95% confidence interval 0.016-0.032); p = 2 × 10−9.
Where it sits Chromosome 3, band 3q12.3 — in an intron of SENP7.
What each result means
C/CNo copy of the version the research linked to Insulin-like growth factor 1 levels. This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Insulin-like growth factor 1 levels. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Insulin-like growth factor 1 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2021 · PMID 33462484 · open access
Questions about rs10511190
What is rs10511190?
rs10511190 is a single position in the genome, in or near the SENP7 gene. Published research associates it with insulin-like growth factor 1 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10511190 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 rs10511190 come from?
GWAS Catalog, Nature genetics 2021, PMID:33462484. 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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