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. 2023 Feb 15;31(6):638–647. doi: 10.1038/s41431-023-01302-2

Table 2.

Mega-sample single variant association analysis with age-related hearing loss traits.

CHR SNP EA EAF Gene H-aid H-diff H-noise H-both
Beta (OR) SE P Beta (OR) SE P Beta (OR) SE P Beta (OR) SE P
1 rs11589562 C 0.424 MAST2 −0.05 (0.95) 0.01 2.25 × 10−8
1 rs2275426 A 0.431 MAST2 −0.05 (0.95) 0.01 3.39 × 10−8
1 rs1707336 G 0.435 MAST2 −0.05 (0.95) 0.01 3.63 × 10−8
1 rs1707304 A 0.436 PIK3R3 −0.05 (0.95) 0.01 2.34 × 10−8 −0.05 (0.95) 0.01 3.30 × 10−8
5 rs537688122a G 7 × 10−4 PDCD6 1.79 (6.0) 0.25 7.06 × 10−11 1.35 (3.9) 0.14 1.04 ×10−21 1.1 (3.0) 0.14 4.96×10−16 1.32 (3.8) 0.15 1.11 × 10−18
5 rs549592074a C 6 × 10−4 PDCD6 1.70 (5.5) 0.28 2.48 × 10−8 1.37 (3.9) 0.16 5.19 × 10−19 1.08 (3.0) 0.15 2.19×10−13 1.32 (3.8) 0.16 6.63 × 10−16
5 rs571370281 G 7 × 10−4 PDCD6 1.71 (5.5) 0.24 1.34 × 10−10 1.31 (3.7) 0.14 1.00 × 10−21 1.04 (2.8) 0.14 1.83×10−15 1.28 (3.6) 0.15 8.00 × 10−19
5 rs7714670 C 0.467 ARHGEF28 0.11 (1.1) 0.02 9.99 × 10−9 0.05 (1.05) 0.01 1.63 × 10−9 0.05 (1.05) 0.01 1.06 × 10−8
5 rs11949860 A 0.462 ARHGEF28 0.11 (1.1) 0.02 3.87 × 10−8 0.05 (1.05) 0.01 9.92 × 10−9
5 rs35525194 G 0.471 ARHGEF28 0.11 (1.1) 0.02 7.03 × 10−9 0.05 (1.05) 0.01 2.19 × 10−9 0.05 (1.05) 0.01 1.21 × 10−8
5 rs6453022 A 0.501 ARHGEF28 0.11 (1.1) 0.02 7.30 × 10−9 0.05 (1.05) 0.01 2.75 × 10−10 0.06 (1.06) 0.01 4.13 × 10−10
5 rs7716253 C 0.524 ARHGEF28 0.11 (1.1) 0.02 8.82 × 10−9 0.05 (1.05) 0.01 6.29 × 10−9 0.05 (1.05) 0.01 2.19 × 10−8
5 rs2973549 A 0.478 ARHGEF28 0.11 (1.1) 0.02 1.23 × 10−8 0.05 (1.05) 0.01 2.22 × 10−8
5 rs2973548 T 0.478 ARHGEF28 0.11 (1.1) 0.02 2.61 × 10−8 0.05 (1.05) 0.01 4.90 × 10−8
6 rs146694394 T 0.005 SYNJ2 0.33 (1.4) 0.06 1.72 × 10−8
6 rs1574430 C 0.608 SLC22A7 0.05 (1.05) 0.01 2.10 × 10−10 0.05 (1.05) 0.01 4.22×10−10 0.06 (1.06) 0.01 8.06 × 10−12
6 rs2242416 G 0.606 CRIP3 0.05 (1.05) 0.01 2.25 × 10−10 0.05 (1.05) 0.01 3.89×10−10 0.06 (1.06) 0.01 8.13 × 10−12
6 rs2254303 A 0.606 CRIP3 0.05 (1.05) 0.01 1.49 × 10−9 0.05 (1.05) 0.01 1.90×10−9 0.06 (1.06) 0.01 3.88 × 10−11
6 rs765264064a C 6 × 10−5 FILIP1 3.01(20.3) 0.48 2.81 × 10−9
6 rs121912560a G 0.005 MYO6 5.28(196.3) 0.98 5.15 × 10−14 3.73 (41.9) 0.87 2.26 × 10−12 3.26 (26.1) 0.86 1.09×10−9 3.86 (47.7) 0.88 8.72 × 10−13
7 rs2286276 T 0.284 TBL2 0.05 (1.05) 0.01 4.66 × 10−8
7 rs61010704 G 0.283 MLXIPL 0.05 (1.05) 0.01 3.16 × 10−8 0.05 (1.05) 0.01 2.72 × 10−8
22 rs371997714 G 0.293 BAIAP2L2 0.05 (1.05) 0.01 1.40 × 10−8
22 rs36062310 A 0.043 KLHDC7B 0.12 (1.1) 0.02 1.32 × 10−9 0.12 (1.3) 0.02 6.66 × 10−9

Genome-wide significant variants (p < 5 × 10−8) with hearing aid (H-aid), hearing difficulty (H-diff), hearing difficulty with background noise (H-noise) and the combined hearing trait (H-both) in the analysis of the mega-sample of white-European individuals from the UK Biobank. The p-values for replicated associations (empirical p-values <0.05 adjusting for variants and traits brought to replication) are shown in bold (See Table S4 for replication analytical and empirical values).

CHR chromosome, EA effect allele, EAF effect allele frequency, OR odds ratio, SE standard error, P p-value.

aVariant not found present in the replication sample.