Standard
Urate levels
INHBC · rs1106766
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 Urate levels — no copies of the reported risk allele. (GWAS Catalog, Circ Cardiovasc Genet 2010, PMID:20884846)
C/T
Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Urate levels. (GWAS Catalog, Circ Cardiovasc Genet 2010, PMID:20884846)
T/T
Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Urate levels compared to the general population. (GWAS Catalog, Circ Cardiovasc Genet 2010, PMID:20884846)
Source
Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors
Yang Q,
Köttgen A,
Dehghan A,
Smith AV,
Glazer NL,
Chen MH,
Chasman DI,
Aspelund T,
Eiriksdottir G,
Harris TB,
Launer L,
Nalls M
and 29 more — show all
Hernandez D,
Arking DE,
Boerwinkle E,
Grove ML,
Li M,
Linda Kao WH,
Chonchol M,
Haritunians T,
Li G,
Lumley T,
Psaty BM,
Shlipak M,
Hwang SJ,
Larson MG,
O'Donnell CJ,
Upadhyay A,
van Duijn CM,
Hofman A,
Rivadeneira F,
Stricker B,
Uitterlinden AG,
Paré G,
Parker AN,
Ridker PM,
Siscovick DS,
Gudnason V,
Witteman JC,
Fox CS,
Coresh J
Circulation. Cardiovascular genetics · 2010 · PMID 20884846
Questions about rs1106766
What is rs1106766?
rs1106766 is a single position in the genome, in or near the INHBC gene. Published research associates it with urate levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs1106766 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 rs1106766 come from?
GWAS Catalog, Circ Cardiovasc Genet 2010, PMID:20884846. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
← See all variants