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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 10,280 European ancestry individuals.
The effect
The reported allele is G; the catalogue records no effect size
; p = 5 × 10−9.
How common The G allele had a frequency of about 65% in the people studied.
Where it sits Chromosome 7, band 7p12.3 — between genes, 16.8 kb from LOC730338.
What each result means
C/CNo copy of the version the research linked to Insulin-like growth factors. This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Insulin-like growth factors. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Insulin-like growth factors. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs700752 is a single position in the genome, in or near the TNS3 gene. Published research associates it with insulin-like growth factors. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs700752 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 rs700752 come from?
GWAS Catalog, Hum Mol Genet 2011, PMID:21216879. 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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