Standard
Insulin-like growth factors
TNS3 · rs700752
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 each result means
C/C
Published research associates this genotype with typical/baseline likelihood of Insulin-like growth factors — no copies of the reported risk allele.
C/G
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Insulin-like growth factors.
G/G
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Insulin-like growth factors compared to the general population.
Source
A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3
Kaplan RC,
Petersen AK,
Chen MH,
Teumer A,
Glazer NL,
Döring A,
Lam CS,
Friedrich N,
Newman A,
Müller M,
Yang Q,
Homuth G
and 25 more — show all
Cappola A,
Klopp N,
Smith H,
Ernst F,
Psaty BM,
Wichmann HE,
Sawyer DB,
Biffar R,
Rotter JI,
Gieger C,
Sullivan LS,
Völzke H,
Rice K,
Spyroglou A,
Kroemer HK,
Ida Chen YD,
Manolopoulou J,
Nauck M,
Strickler HD,
Goodarzi MO,
Reincke M,
Pollak MN,
Bidlingmaier M,
Vasan RS,
Wallaschofski H
Human molecular genetics · 2011 · PMID 21216879
Questions about rs700752
What is rs700752?
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.
← See all variants