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Table 2 Minor allelic, genotypic, and haplotype distributions of UGT1A1 polymorphism in studied patients (N = 69)

From: UGT1A1 mutation association with increased bilirubin levels and severity of unconjugated hyperbilirubinemia in ABO incompatible newborns of China

UGT1A1 polymorphism

Location

N

Frequency

PH-Wa

TATA box (rs8175347)

promoter

  

1

TA7

 

9

0.07

 

TA6

 

129

0.93

 

TA7/TA7

 

0

0

 

TA6/TA7

 

9

0.13

 

TA6/TA6

 

60

0.87

 

C.211 G > A (rs4148323)

Exon 1

  

1

A

 

21

0.15

 

G

 

117

0.85

 

A/A

 

1

0.01

 

G/A

 

19

0.28

 

G/G

 

49

0.71

 

c.1091 C > T (rs34946978)

Exon 4

  

1

T

 

3

0.02

 

C

 

135

0.98

 

T/T

 

0

0

 

C/T

 

3

0.04

 

C/C

 

66

0.96

 

Haplotype (rs8175347-rs4148323-rs34946978)

TA6GC

  

0.76

 

TA6AC

  

0.15

 

TA7GC

  

0.065

 

TA6GT

  

0.018

 

TA6AT

  

0.0037

 
  1. aHardy-Weinberg Equilibrium test p value