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Table 3 Genotype frequencies for the -838C>A, -79C>T, and V109G p27kip1 single-nucleotide polymorphisms (SNPs).

From: A single-nucleotide polymorphism in the human p27kip1gene (-838C>A) affects basal promoter activity and the risk of myocardial infarction

 

-838C>A*

 

CC

CA

AA

Patients

47 (26%)

88 (49%)

45 (25%)

Controls

95 (38%)

115 (46%)

40 (16%)

 

-79C>T

 

CC

CT

TT

Patients

99 (55%)

70 (39%)

11 (6%)

Controls

152 (61%)

82 (32%)

16 (7%)

 

V109G

 

VV

VG

GG

Patients

100 (55%)

71 (40%)

9 (5%)

Controls

143 (57%)

98 (39%)

9 (4%)

  1. *P = 0.009; OR = 1.73, 95%CI = 1.12–2.70 (AA+AC) vs CC. For each SNP, the table shows the total number of cases for each genotype and their relative frequencies among controls and patients with myocardial infarction.
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BMC Biology

ISSN: 1741-7007

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