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. 2005 Jun 7;93(2):260–265. doi: 10.1038/sj.bjc.6602658

Table 1. Standardised incidence ratios (SIRs) for breast cancer in 712 unaffected female blood relatives of 75 patients with ataxia telangiectasia (AT) from 66 Nordic families by familial relationship and probability of carrying an ATM mutation.

      Breast cancer
Female relative No. Person-years at risk Obs Exp SIR 95% CI
All 712 22 892 34 19.51 1.7 1.2–2.4
             
Familial relationship            
 Mothera 64 1330 8 1.20 6.7 2.9–13
 Other female relatives 648 21 562 26 18.31 1.4 0.9–2.1
  Sister of proband 39 871 0 0.05
  Grandmother 94 3502 8 4.87 1.6 0.7–3.2
  Aunt 121 5488 2 3.24 0.6 0.1–2.2
  Great-grandmother 89 2340 8 3.89 2.1 0.9–4.1
  Grandmother's sister 118 4357 7 5.43 1.3 0.5–2.8
  Female cousin 187 5004 1 0.83 1.2 0.0–6.7
             
Mutation carrier probabilityb            
 1c 72 1720 8 1.81 4.4 1.9–8.7
 0.67; 0.50; 0.25 589 19 628 24 15.39 1.6 1.0–2.2
  0.67; 0.50 252 9709 10 8.13 1.2 0.6–2.3
  0.25 337 9919 14 7.33 1.9 1.0–3.2
 Backgroundd 51 1545 2 2.31 0.9 0.1–3.2

Obs=observed cancers; Exp=expected cancers; CI=confidence interval.

a

The mother was not known in each of two Swedish families.

b

The estimated mutation carrier probability on an individual, according to the location in the pedigree, including information on consanguinity combined with the outcome of any relevant gene testing of relatives (see also text).

c

Two mothers regarded as carriers of a wild-type allele were excluded from this group.

d

Relatives who married into consanguineous families, or relatives in branches of the family not involved in the gene transmission.