Table 1

Summary results for rs210134 and rs210142 SNPs associated with CLL risk

SNPPosition, bpRisk alleleUK-GWAS
SF-GWAS
GEC-GWAS
Replication
Combined
RAFOR (95% CI)PtrendRAFOR (95% CI)PtrendRAFOR (95% CI)PtrendRAFOR (95% CI)PtrendOR (95% CI)PtrendPhet (I2)
rs210134 33 648 187 0.68 1.31 (1.13-1.51) 2.95 × 10−4 0.69 1.56 (1.21-2.02) 6.39 × 10−4 0.70* 1.37 (1.08-1.75)* .0096* 0.68 1.35 (1.19-1.54) 4.87 × 10−6 1.37 (1.22-1.53) 1.03 × 10−12 .50 (0%) 
rs210142 33 654 815 0.70* 1.35 (1.17-1.57)* 6.82 × 10−5* 0.70* 1.58 (1.22-2.05)* 5.44 × 10−4* 0.70* 1.38 (1.09-1.76)* .0077* 0.69 1.47 (1.28-1.68) 2.41 × 10−8 1.40 (1.25-1.57) 9.47 × 10−16 .59 (0%) 
SNPPosition, bpRisk alleleUK-GWAS
SF-GWAS
GEC-GWAS
Replication
Combined
RAFOR (95% CI)PtrendRAFOR (95% CI)PtrendRAFOR (95% CI)PtrendRAFOR (95% CI)PtrendOR (95% CI)PtrendPhet (I2)
rs210134 33 648 187 0.68 1.31 (1.13-1.51) 2.95 × 10−4 0.69 1.56 (1.21-2.02) 6.39 × 10−4 0.70* 1.37 (1.08-1.75)* .0096* 0.68 1.35 (1.19-1.54) 4.87 × 10−6 1.37 (1.22-1.53) 1.03 × 10−12 .50 (0%) 
rs210142 33 654 815 0.70* 1.35 (1.17-1.57)* 6.82 × 10−5* 0.70* 1.58 (1.22-2.05)* 5.44 × 10−4* 0.70* 1.38 (1.09-1.76)* .0077* 0.69 1.47 (1.28-1.68) 2.41 × 10−8 1.40 (1.25-1.57) 9.47 × 10−16 .59 (0%) 

RAF indicates risk allele frequencies (based on control data).

*

Imputed genotype.

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