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. 2019 Jul 23;8(8):1224–1229. doi: 10.1530/EC-19-0225

Table 2.

Distribution of 89 BRCA1/2-associated MBC cases and 157 unaffected male BRCA1/2 mutation carriers according to genotype frequencies of CYP1A1 rs743572, CYP1B1 rs1056836 and rs1800440 and MBC risk estimates.

Polymorphism Genotype BRCA1/2 MBC cases (n = 89) Unaffected male BRCA1/2 mutation carriers (n = 157) OR (95% CI) P value
n % n %
CYP17A1 c.-34T>C TT 31 34.8 57 36.3 Ref
rs743572 TC 48 53.9 71 45.2 1.08 (0.53–2.20) 0.83
CC 10 11.3 29 18.5 0.81 (0.29–2.23) 0.68
Co-dominant 0.94 (0.59–1.50) 0.79
CYP1B1 p.Leu432Val GG 34 38.2 67 42.7 Ref
rs1056836 GC 44 49.4 70 44.6 1.42 (0.71–2.86) 0.32
CC 11 12.4 20 12.7 0.62 (0.20–1.92) 0.41
Co-dominant 0.95 (0.59–1.54) 0.83
CYP1B1 p.Asn453Ser AA 53 59.5 96 61.2 Ref
rs1800440 AG 32 36.0 55 35.0 1.44 (0.72–2.91) 0.31
GG 4 4.5 6 3.8 2.97 (0.71–12.38) 0.13
Co-dominant 1.57 (0.91–2.73) 0.11