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Table 3 NOS3 gene promoter haplotypes, number of copies, and prostate cancer risk.

From: The -786T>C promoter polymorphism of the NOS3gene is associated with prostate cancer progression

Haplotypesa

(SSCP Conformation)

Units

Zero Copies

One Copy

p-Value

Two copies

p-Value

No mutations

(T)

Controls/cases

17/16

48/36

0.73

29/30

1.0

 

OR (95% CI)

1.00 (ref)

0.80 (0.36 – 1.79)

 

1.10 (0.47 – 2.58)

 

[-786T>C; -714G>T; -690C>T]

(C)

Controls/cases

42/36

44/37

0.92

8/9

0.81

 

OR (95% CI)

1.00 (ref)

0.98 (0.52–1.83)

 

1.31 (0.46 – 3.76)

 

[-786T>C; -764A>G; -690C>T]

(A)

Controls/cases

72/71

22/11

0.13

0/2

--

 

OR (95% CI)

1.00 (ref)

0.51 (0.23 – 1.12)

 

--

 

[-786T>C; -690A>G; -649G>A]b

(N)

Controls/cases

94/82

0/1

--

0/0

--

 

OR (95% CI)

1.00 (ref)

--

 

--

 
  1. (a) Alleles listed for dbSNP ID (GenBank) in 5' to 3' order: NM_2070744, NM_EF042808, NM_EF042809, NM_3918225, NM_EF042810.
  2. (b) Haplotype that appear only once between groups (PCa and BPH).
  3. CI: confidence interval/OR: odds ratio
  4. (--) inapplicable data