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. 2017 Mar 30;12(3):e0174778. doi: 10.1371/journal.pone.0174778

Table 4. Allele and genotype frequencies of H63D and C282Y HFE polymorphisms in our previous study1 and TCGA GBM (TP, NB) samples1, stratified by gender.

PSHCI GBM (n = 97)2 TP (n = 264) NB (n = 261)
Male (n = 49) Female (n = 48) Male (n = 167) Female (n = 97) Male (n = 164) Female (n = 97)
Genotype
H63D/+ 9 (18.4%) 9 (18.8%) 40 (24.0%) 21 (21.6%) 39 (23.8%) 21 (21.6%)
H63D/H63D 0 (0.0%) 1 (2.1%) 4 (2.4%) 2 (2.1%) 4 (2.4%) 2 (2.1%)
C282Y/+ 2 (4.1%) 4 (8.3%) 9 (5.4%) 6 (6.2%) 9 (5.5%) 7 (7.2%)
C282Y/C282Y 0 (0.0%) 0 (0.0%) 2 (1.2%) 0 (0.0%) 1 (0.6%) 0 (0.0%)
H63D/C282Y 0 (0.0%) 0 (0.0%) 2 (1.2%) 1 (1.0%) 2 (1.2%) 1 (1.0%)
+/+ 38 (77.6%) 34 (70.8%) 110 (65.9%) 67 (69.1%) 109 (66.5%) 66 (68.0%)
Alleles
H63D 9/98 (9.2%) 11/96 (11.5%) 50/334 (15.0%) 26/194 (13.4%) 49/328 (14.9%) 26/194 (13.4%)
C282Y 2/98 (2.0%) 4/96 (4.2%) 15/334 (4.5%) 7/194 (3.6%) 13/328 (4.0%) 8/194 (4.1%)

1 Caucasian only, Values were expressed as n = N (%) or n = N

2 Lee SY, et al. J Neurooncol. 2015; 122: 97–104.