Back to Search
Start Over
Common variation at 10p12.31 near MLLT10 influences meningioma risk.
- Source :
-
Nature genetics [Nat Genet] 2011 Jul 31; Vol. 43 (9), pp. 825-7. Date of Electronic Publication: 2011 Jul 31. - Publication Year :
- 2011
-
Abstract
- To identify susceptibility loci for meningioma, we conducted a genome-wide association study of 859 affected individuals (cases) and 704 controls with validation in two independent sample sets totaling 774 cases and 1,764 controls. We identified a new susceptibility locus for meningioma at 10p12.31 (MLLT10, rs11012732, odds ratio = 1.46, P(combined) = 1.88 × 10(-14)). This finding advances our understanding of the genetic basis of meningioma development.<br />Competing Interests: Statement The authors declare no competing financial interests.
- Subjects :
- Genetic Loci
Genome-Wide Association Study
Humans
Male
Meningeal Neoplasms epidemiology
Meningioma epidemiology
Polymorphism, Genetic
Polymorphism, Single Nucleotide
Risk
Chromosomes, Human, Pair 10 genetics
Genetic Predisposition to Disease
Meningeal Neoplasms genetics
Meningioma genetics
Transcription Factors genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1546-1718
- Volume :
- 43
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- Nature genetics
- Publication Type :
- Academic Journal
- Accession number :
- 21804547
- Full Text :
- https://doi.org/10.1038/ng.879