Skip to main content
. 2019 Aug 24;8(9):1306. doi: 10.3390/jcm8091306

Table 2.

Alleles and genotypes frequencies for ESR1 c.454-397T>C (PvuII) polymorphism.

ESR1 c.397T>C (PvuII)
Genotype Frequencies (%) Allele Frequencies (%)
TT TC CC T
* 1000Genomes: 57.7%
C
* 1000Genomes: 42.3%
IBD (all patients) n = 198 77 (38.9%) 81 (41.0%) 40 (20.2%) 235 (59.3%) 161 (40.7%)
UC patients (n = 98) 29 (29.6%) 46 (46.9%) 23 (23.5%) 104 (53.1%) 92 (46.9%)
CD patients ** (n = 100) 48 (48.0%) 35 (35.0%) 17 (17.0%) 131 (65.5%) 69 (34.5%)
CG (n = 41) 13 (31.7%) 24 (58.5%) 4 (9.8%) 50 (61.0%) 32 (39.0%)
Comparisons of allelic and genotypic frequencies between groups under study
[TT + TC] vs. [CC] [TT] vs. [TC + CC] [TT] vs. [CC] [T] vs. [C] [C] vs. [T]
CG vs. IBD
OR, 95% CI
P-value
OR = 0.43
[0.14–1.27]
P = 0.116
OR = 0.73
[0.36–1.50]
P = 0.388
OR = 1.69
[0.517–5.516]
P = 0.382
OR = 1.07
[0.66–1.74]
OR = 0.93
[0.57–1.52]
P = 0.784
CG vs. UC
OR, 95% CI
P-value
OR = 0.35
[0.11–1.09]
P = 0.062
OR = 1.11
[0.50–2.43]
P = 0.804
OR = 2.58
[0.74–8.97]
P = 0.129
OR = 1.38
[0.82–2.34]
OR = 0.72
[0.43–1.22]
P = 0.226
CG vs. CD
OR, 95% CI
P-value
OR = 0.58
[0.17–1.68]
P = 0.273
OR = 0.50
[ 0.13–0.70]
P = 0.004
OR = 1.15
[0.33–4.02]
P = 0.825
OR = 0.82
[0.48–1.40]
OR = 1.22
[0.72–2.10]
P = 0.472
CD vs. UC
OR, 95% CI
P-value
OR = 0.67
[0.33–1.35]
P = 0.257
OR = 2.20
[ 1.22–3.94]
P = 0.008
OR = 2.24
[ 1.03–4.88]
P = 0.041
OR = 1.68
[1.12–2.52]
OR = 0.60
[ 0.40–0.89]
P = 0.012

In bold were marked statistically significant results (P-value < 0.05). No corrections for the multiple statistical testing were made. CG—control group, [TT+TC] vs. [CC]—dominant model, risk allele: T, [TT] vs. [TC+CC]—recessive model, risk allele: C, * Allele frequencies for European population according to 1000 Genomes Project have been gathered from https://www.ncbi.nlm.nih.gov/projects/SNP/snp_ss.cgi?ss=ss1322898669 website [41]. ** HWE analysis revealed discordance in CD patients group.