Table III.

PIN1 −842G>C and −667T>C haplotypes and SCCHN risk

Haplotypes	Cases (2012 alleles),n (%)	Controls (2014 alleles),n (%)	OR (95% CI)a	P
−842G–667T	1326 (65.9)	1328 (65.9)	1.00 (Ref.)	Ref.
−842G–667C	509 (25.3)	462 (23.0)	1.23 (0.90–1.67)	0.190
−842C–667C	175 (8.7)	198 (9.8)	0.81 (0.52–1.27)	0.360
−842C–667T	2 (0.1)	26 (1.3)	0.003 (0.001–0.16)	0.005
	P = 0.00002b

^aAdjusted for age, sex, smoking status, and alcohol use.

^bGlobal test.