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. 2023 Apr 12;11(4):1155. doi: 10.3390/biomedicines11041155

Table 1.

Multivariate analysis, adjusted for age, sex, and smoking habits, comparing SNPs of NR3C1 (rs6198, rs104893913, rs104893909, and rs104893911) in 384 Graves’ disease patients and 408 controls.

SNP Controls, N (%) Cases, N (%) p Value OR 95% CI
NR3C1 rs6198
Genotypes

TT

280 (68.6)

301 (78.4)
0.0038 1.627 1.170–2.264
TC 120 (29.4) 80 (20.8)
CC 8 (2.0) 3 (0.6)
Alleles T 680 (83.3) 682 (88.8) 0.0017 1.586 1.187–2.128
C 136 (16.7) 86 (11.2)
NR3C1 rs104893913
Genotypes

CC

408 (100)

384 (100)

N/A

N/A

N/A
CT 0 (0) 0 (0)
TT 0 (0) 0 (0)
Alleles C
T
816 (100)
0 (0)
768 (100)
0 (0)
N/A N/A N/A
NR3C1 rs104893909
Genotypes

AA

408 (100)

384 (100)

N/A

N/A

N/A
AT 0 (0) 0 (0)
TT 0 (0) 0 (0)
Alleles A
T
816 (100)
0 (0)
768 (100)
0 (0)
N/A N/A N/A
NR3C1 rs104893911
Genotypes

AA

408 (100)

384 (100)

N/A

N/A

N/A
AG 0 (0) 0 (0)
GG 0 (0) 0 (0)
Alleles A
G
816 (100)
0 (0)
768 (100)
0 (0)
N/A N/A N/A

SNP rs6198—TT = wild-type; TC = heterozygous; CC = polymorphic. SNP rs104893913—CC = wild-type; CT = heterozygous; TT = polymorphic. SNP rs104893909—AA = wild-type; AT = heterozygous; TT = polymorphic.