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Hum Mol Genet ; 25(12): 2612-2620, 2016 06 15.
Article in English | MEDLINE | ID: mdl-27008869

ABSTRACT

Endometrial cancer is the most common gynecological malignancy in the developed world. Although there is evidence of genetic predisposition to the disease, most of the genetic risk remains unexplained. We present the meta-analysis results of four genome-wide association studies (4907 cases and 11 945 controls total) in women of European ancestry. We describe one new locus reaching genome-wide significance (P < 5 × 10 -8) at 6p22.3 (rs1740828; P = 2.29 × 10 -8, OR = 1.20), providing evidence of an additional region of interest for genetic susceptibility to endometrial cancer.


Subject(s)
Endometrial Neoplasms/genetics , Genetic Predisposition to Disease , Genome-Wide Association Study , Chromosomes, Human, Pair 6/genetics , Endometrial Neoplasms/pathology , Female , Genotype , Humans , Polymorphism, Single Nucleotide , White People/genetics
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