Table 3. Prostate cancer genotype specific risk for two SNPs in BRIP1/FANCJ genomic region.

	GG	TG	TT	Per allele OR (95% CI)	OR Hom (95% CI)	OR Het (95% CI)	P Het	P trend
rs6504074
Familial	345	274	64	1.20 (1.04–1.37)	1.57 (1.13–2.17)	1.13 (0.94–1.35)	0.21	0.01
Young	618	453	87	1.07 (0.94–1.20)	1.19 (0.89–1.59)	1.04 (0.89–1.21)	0.62	0.28
All	963	727	151	1.11 (1.00–1.23)	1.33 (1.03–1.71)	1.07 (0.94–1.23)	0.32	0.04
Control	1031	727	122
rs8076727
Familial	373	261	46	1.20 (1.04–1.38)	1.39 (0.96–2.00)	1.21 (1.01–1.46)	0.04	0.01
Young	658	432	72	1.12 (1.00–1.27)	1.23 (0.90–1.69)	1.14 (0.98–1.33)	0.10	0.06
All	1031	693	118	1.13 (1.03–1.28)	1.29 (0.97–1.70)	1.17 (1.017–1.336)	0.03	0.01
Control	1124	648	100

OR=odds ratio; SNP=single nucleotide polymorphism.