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Table 2 CHEK2 mutations were more frequent in cases than in controls

From: CHEK2 contribution to hereditary breast cancer in non-BRCAfamilies

CHEK2mutation type

Controls

(n= 1,026)a

Allelic frequency in controls

Cases

(n= 1,014)a

Allelic frequency in cases

P value

OR

95% CI

Any CHEK2 mutation

4

0.39%

16

1.58%

0.0065

4.15

(1.38 to 12.50)

CHEK2 deleterious mutations

3

0.29%

15

1.48%

0.0042

5.18

(1.49 to 18.00)

  1. an indicates the number of alleles.