Dataset
The most significant SNPs in the transport pathway genes and risk of EOC by histology, invasiveness, and race/ethnicity1.
Affiliations
Organisations
- (1) University of Cambridge, grid.5335.0
- (2) Moffitt Cancer Center, grid.468198.a
- (3) N.N. Alexandrov National Cancer Centre, grid.477553.7
- (4) Memorial Sloan Kettering Cancer Center, grid.51462.34
- (5) Hannover Medical School, grid.10423.34
- (6) University of Southern California, grid.42505.36
- (7) Roswell Park Cancer Institute, grid.240614.5
- (8) German Cancer Research Center, grid.7497.d
- (9) University of Toronto, grid.17063.33
- (10) Cedars-Sinai Medical Center, grid.50956.3f
Countries
Continents
Description
1 INV: all invasive EOC combined; LMP: low malignant potential / borderline tumors; SER: serous; CC: clear cell; End: endometrioid; Muc: mucinous. Statistically significant associations are indicated in bold (P<0.05). Data format is the following: OR (95% CI); p-value; FDR q-value (white-European women). Only significant FDRs (q<0.2) are shown (HEPH: INV and SER; UGT1A: End).The most significant SNPs in the transport pathway genes and risk of EOC by histology, invasiveness, and race/ethnicity1.