failed to reach significancep =0.1869
The TT homozygous variant genotype was associated with a 1.43-fold increased BCa risk; however, this result also failed to reach significance (95%CI=0.88-2.36, p =0.1869, Table II, top panel).
The TT homozygous variant genotype was associated with a 1.43-fold increased BCa risk; however, this result also failed to reach significance (95%CI=0.88-2.36, p =0.1869, Table II, top panel).