Skip to main content

Table 4 Genotypes and allele frequencies of SNPs in the UGT1A1, SLCO1B1, SLCO1B3, BLVRA, and HMOX1 genes

From: Associations between UGT1A1, SLCO1B1, SLCO1B3, BLVRA and HMOX1 polymorphisms and susceptibility to neonatal severe hyperbilirubinemia in Chinese Han population

Genotypes/Alleles

Case group (n = 144)

n (%)

Control group (n = 50)

n (%)

P value

OR (95%CI)

UGT1A1-rs4148323

    

GG

73 (50.7)

37 (74.0)

 

1

GA

55 (38.2)

13 (26.0)

0.036

2.144 (1.041–4.416)

AA

16 (11.1)

0 (0)

0.003*

0.820 (0.744–0.904)

A allele

87 (30.2)

13 (13.0)

  

G allele

201 (69.8)

87 (87.0)

0.001

2.897 (1.535–5.465)

UGT1A1-rs3771341

    

GG

134 (93.1)

42 (84.0)

 

1

GA

9 (6.2)

7 (14.0)

0.129*

0.403 (0.141–1.148)

AA

1 (0.7)

1 (2.0)

0.426*

0.313 (0.019–5.120)

A allele

11 (3.8)

9 (9.0)

  

G allele

277 (96.2)

91 (91.0)

0.063

0.402 (0.161-1.000)

UGT1A1-rs34946978

    

CC

136 (94.4)

48 (96.0)

  

CT

8 (5.6)

2 (4.0)

1.000*

1.412 (0.290–6.882)

C allele

280 (97.2)

98 (98.0)

  

T allele

8 (2.8)

2 (2.0)

1.000*

0.714 (0.149–3.421)

UGT1A1-rs114982090

    

CC

138 (95.8)

50 (100.0)

  

CT

6 (4.2)

0 (0)

0.342*

0.958 (0.926–0.992)

C allele

282 (97.9)

100 (100.0)

  

T allele

6 (2.1)

0 (0)

0.345*

0.979 (0.963–0.996)

SLCO1B1-rs4149056

    

TT

118 (81.9)

41 (82.0)

 

1

CT

25 (17.4)

9 (18.0)

0.934

0.965 (0.416–2.237)

CC

1 (0.7)

0 (0)

1.000*

0.992 (0.975–1.008)

C allele

27 (9.4)

9 (9.0)

  

T allele

261 (90.6)

91 (91.0)

0.911

1.046 (0.474–2.308)

SLCO1B1-rs1564370

    

CC

89 (61.8)

34 (68.0)

 

1

CG

48 (33.3)

13 (26.0)

0.354

0.709 (0.342–1.470)

GG

7 (4.9)

3 (6.0)

1.000*

1.122 (0.274–4.591)

C allele

226 (78.5)

81 (81.0)

  

G allele

62 (21.5)

19 (19.0)

0.669

0.855 (0.482–1.517)

SLCO1B3- rs2417940

    

CC

117 (81.3)

29 (58.0)

 

1

CT

27 (18.7)

20 (40.0)

0.002

2.989 (1.474–6.060)

TT

0 (0)

1 (2.0)

0.204*

1.034 (0.968–1.106)

C allele

261 (90.6)

78 (78.0)

  

T allele

27 (9.4)

22 (22.0)

0.001

2.726 (1.471–5.054)

SLCO1B3-rs2117032

    

CC

23 (16.0)

8 (16.0)

 

1

CT

66 (45.8)

30 (60.0)

0.565

1.307 (0.524–3.256)

TT

55 (38.2)

12 (24.0)

0.367

0.627 (0.227–1.737)

C allele

112 (38.9)

46 (46.0)

  

T allele

176 (61.1)

54 (54.0)

0.212

0.747 (0.472–1.182)

BLVRA- rs699512

    

AA

73 (50.7)

27 (54.0)

 

1

GA

60 (41.7)

18 (36.0)

0.550

0.811 (0.408–1.613)

GG

11 (7.6)

5 (10.0)

0.766*

1.229 (0.391–3.864)

A allele

206 (71.5)

72 (72.0)

  

G allele

82 (28.5)

28 (28.0)

0.928

0.977 (0.589–1.620)

HMOX1- rs2071747

    

GC

13 (9.0)

2 (4.0)

  

GG

131 (91.0)

48 (96.0)

0.362*

2.382 (0.518–10.944)

C allele

13 (4.5)

2 (2.0)

  

G allele

275 (95.5)

98 (98.0)

0.372*

2.316 (0.514–10.448)

  1. *: Fisher’s precision probability test