Haplotype

n(%)

P

OR(95%CI)

Case

Control

Block 1

 

 

 

 

AAGTGGACC

36.18(6.1)

58.09(7.1)

0.477

0.86(0.56~1.32)

AAGTGGACT

53.22(9.0)

79.30(9.6)

0.675

0.93(0.64~1.33)

ACCCAAGCC

238.96(40.2)

329.06(40.0)

0.900

1.01(0.82~1.26)

ACGCGGGCC

36.91(6.2)

38.03(4.6)

0.182

1.37(0.86~2.19)

ACGCGGGCT

109.43(18.4)

162.98(19.8)

0.526

0.92(0.70~1.20)

ACGCGGGTC

28.99(4.9)

43.25(5.3)

0.759

0.93(0.57~1.50)

TAGTGAGCC

20.00(3.4)

15.95(1.9)

0.090

1.77(0.91~3.45)

TAGTGGACC

44.59(7.5)

62.46(7.6)

0.963

0.99(0.66~1.48)

Block 2

 

 

 

 

CCCT

99.94(17.2)

132.48(16.6)

0.843

1.03(0.77~1.37)

CGCC

283.36(48.7)

403.93(50.5)

0.366

0.91(0.73~1.12)

CGTC

104.90(18.0)

119.08(14.9)

0.142

1.24(0.93~1.66)

TGCC

78.26(13.4)

113.54(14.2)

0.626

0.93(0.68~1.26)


Block 1: The variant alleles of VEGF: rs1547651, rs699947, rs2010963, rs1005230, rs735286, rs833068, rs833070, rs3024994 and rs3025007.
Block 2: The variant alleles of VEGF: rs3025021, rs3025030, rs3025035 and rs3025039.
Table 2: Frequency distribution of VEGF haplotype alleles between the cases and the controls and their associations with risk of GC.
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