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. Author manuscript; available in PMC: 2010 Mar 1.
Published in final edited form as: Prostate. 2009 Mar 1;69(4):363–372. doi: 10.1002/pros.20887

Table III.

Population attributable risk percent (PAR%) for SNPs in the 8q24, 17q12, and 17q24.3 chromosomal regions

Variable or SNP Associated risk group Frequency of associated factor (%) PAR% Adjusted PAR%*
Cases Controls 3% Prevalence 5% Prevalence
1st degree family history of PC Yes 20.9 10.8 12.5 11.8 11.0
rs4430796 AA 32.9 25.0 9.7 9.4 9.1
rs1859962 GG 27.3 23.2 5.4 5.3 5.2
rs6983561 CC+CA 11.1 6.5 4.7 4.5 4.3
rs6983267 GG+GT 80.8 75.1 20.4 19.8 19.0
rs1447295 AA+AC 25.2 19.4 6.2 6.0 5.8
All five SNPs All 0.3 0.1 39.2 38.1 37.0
All five SNPs and family history All 0.1 0 46.7 45.4 45.0
*

PAR% adjusted for inflation due to estimating relative risk using the odds ratios, at the indicated probability of being diagnosed with prostate cancer.

Men with five at-risk genotypes.

Men with five at-risk genotypes plus a positive family history of prostate cancer.