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. 2017 Dec 1;8:1892. doi: 10.1038/s41467-017-00320-1

Table 1.

Summary results for newly identified risk loci

Nearest genea Risk allele (frequency) Discovery GWAS meta-analysis UK Replication 1 UK Replication 2 Meta-analysis
Position (hg19, bp) P-value OR (95% CI) P-value OR (95% CI) P-value OR (95% CI) P-value OR (95% CI) I2 (%) P het
3q28, rs4459895 LPP A (0.20) 187954414
 cHL 4.16 × 10−10 1.27 (1.18–1.36) 6.85 × 10−9 1.44 (1.27–1.63) 0.02 1.26 (1.04–1.52) 4.45 × 10−18 1.30 (1.23–1.38) 13 0.33
 NSHL 9.16 × 10−9 1.37 (1.23–1.53) 1.37 × 10−8 1.43 (1.26–1.62) 0.04 1.30 (1.02–1.66) 9.43 × 10−17 1.39 (1.28–1.50) 0 0.93
 MCHL 0.92 1.04 (0.91–1.19) 0.98 1.00 (0.68–1.47) 0.55 1.04 (0.92–1.19) 0 0.82
6q22.33, rs9482849 PTPRK C (0.17) 128288536
 cHL 5.02 × 10−8 1.24 (1.15–1.35) 0.13 1.11 (0.97–1.27) 0.13 1.17 (0.95–1.43) 1.52 × 10−8 1.20 (1.13–1.28) 3 0.39
 NSHL 2.91 × 10−6 1.32 (1.17–1.48) 0.17 1.10 (0.96–1.25) 0.20 1.19 (0.91–1.54) 4.13 × 10−6 1.21 (1.12–1.33) 10 0.35
 MCHL 0.17 1.11 (0.96–1.28) 0.78 1.06 (0.70–1.61) 0.16 1.10 (0.96–1.26) 0 0.97
6q23.3, rs6928977 AHI1 G (0.57) 135626348
 cHL 1.66 × 10−8 1.18 (1.12–1.26) 0.01 1.14 (1.03–1.26) 0.05 1.16 (1.00–1.34) 1.24 × 10−10 1.17 (1.12–1.23) 0 0.85
 NSHL 9.34 × 10−10 1.31 (1.20–1.42) 0.03 1.12 (1.01–1.24) 0.01 1.30 (1.06–1.58) 4.62 × 10−11 1.23 (1.16–1.31) 26 0.25
 MCHL 0.24 1.06 (0.96–1.18) 0.69 1.06 (0.79–1.42) 0.22 1.06 (0.96–1.17) 0 0.22
10p14, rs3781093 GATA3 T (0.88) 8101927
 cHL 4.89 × 10−12 1.35 (1.23–1.47) 4.00 × 10−4 1.32 (1.25–1.44) 0.11 1.21 (0.96–1.52) 4.91 × 10−12 1.28 (1.19–1.37) 64 0.01
 NSHL 9.16 × 10−12 1.53 (1.36–1.75) 2.00 × 10−4 1.44 (1.31–1.61) 0.64 0.92 (0.68–1.26) 9.49 × 10−13 1.39 (1.28–1.53) 61 0.06
 MCHL 0.03 1.18 (1.02–1.36) 0.05 1.56 (1.02–2.40) 0.16 0.91 (0.79–1.04) 73 0.03
13q34, rs112998813 UPF3A C (0.08) 115059729
 cHL 3.63 × 10−3 1.19 (1.06–1.33) 0.03 1.23 (1.03–1.47) 0.43 1.12 (0.84–1.50) 2.70 × 10−4 1.19 (1.08–1.30) 13 0.32
 NSHL 8.43 × 10−8 1.58 (1.34–1.88) 0.03 1.22 (1.02–1.47) 0.28 1.23 (0.85–1.78) 4.58 × 10−8 1.39 (1.23–1.56) 27 0.24
 MCHL 0.92 0.99 (0.80–1.22) 0.27 1.35 (0.80–2.23) 0.75 1.03 (0.85–1.25) 0 0.56
16p13.13, rs34972832 CLEC16A A (0.18) 11198938
 cHL 1.45 × 10−4 1.15 (1.07–1.23) 6.34 × 10−3 1.18 (1.05–1.34) 0.10 1.17 (0.97–1.42) 8.03 × 10−7 1.16 (1.09–1.23) 6 0.37
 NSHL 7.47 × 10−7 1.24 (1.15–1.34) 6.53 × 10−3 1.30 (1.17–1.45) 0.28 1.15 (0.89–1.50) 2.12 × 10−8 1.24 (1.15–1.34) 37 0.18
 MCHL 0.65 0.97 (0.85–1.11) 0.91 1.02 (0.69–1.52) 0.70 0.98 (0.86–1.10) 0 0.94

The risk allele is the allele corresponding to the estimated odds ratio. Frequency of the risk allele is from the CEU population from 1000 Genomes Project

cHL classical Hodgkin lymphoma, NSHL nodular sclerosis Hodgkin lymphoma, MCHL mixed cellularity Hodgkin lymphoma, bp base pair, OR odds ratio, CI confidence interval, I2 proportion of the total variation due to heterogeneity

I2 value ≥ 75% is considered to be characteristic of large heterogeneity

aNearest gene may not be the functional gene