Dataset

The most significant SNPs in the transport pathway genes and risk of EOC by histology, invasiveness, and race/ethnicity1.

public-library-of-science,

2015

DOI:10.1371/journal.pone.0128106.t001, Dimensions: 1455551,

Authors

Dicks, Ed (1)

Affiliations

Organisations

  1. (1) University of Cambridge, grid.5335.0
  2. (2) Moffitt Cancer Center, grid.468198.a
  3. (3) N.N. Alexandrov National Cancer Centre, grid.477553.7
  4. (4) Memorial Sloan Kettering Cancer Center, grid.51462.34
  5. (5) Hannover Medical School, grid.10423.34
  6. (6) University of Southern California, grid.42505.36
  7. (7) Roswell Park Cancer Institute, grid.240614.5
  8. (8) German Cancer Research Center, grid.7497.d
  9. (9) University of Toronto, grid.17063.33
  10. (10) Cedars-Sinai Medical Center, grid.50956.3f

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.