Table 3.
Strata | Chromosome | SNP | Position | Gene | Allelea | EAF | OR (95%CI) | P-value |
---|---|---|---|---|---|---|---|---|
Lung | 1p31.1 | rs71658797 | 77967507 | FUBP1 | T_A | 0.099 | 1.12 (0.99–1.27) | 7.54 × 10−2 |
Lung | 6q27 | rs6920364 | 167376466 | RNASET2 | G_C | 0.449 | 1.08 (1.00–1.17) | 5.25 × 10−2 |
Lung | 8p21.1 | rs11780471 | 27344719 | EPHX2, CHRNA2 | G_A | 0.063 | 0.80 (0.67–0.95) | 1.00 × 10−2 |
Lung | 13q13.1 | rs11571833 | 32972626 | BRCA2 | A_T | 0.010 | 1.66 (1.14–2.41) | 7.78 × 10−3 |
Lung | 15q21.1 | rs66759488 | 47577451 | SEMA6D | G_A | 0.362 | 1.05 (0.97–1.14) | 1.91 × 10−1 |
Lung | 15q25.1 | rs55781567 | 78857986 | CHRNA5 | C_G | 0.366 | 1.31 (1.21–1.41) | 1.69 × 10−11 |
Lung | 19q13.2 | rs56113850 | 41353107 | CYP2A6 | C_T | 0.429 | 0.91 (0.83–0.99) | 2.86 × 10−2 |
Adeno | 3q28 | rs13080835 | 189357199 | TP63 | G_T | 0.489 | 0.96 (0.86–1.08) | 5.28 × 10−1 |
Adeno | 5p15.33 | rs7705526 | 1285974 | TERT | C_A | 0.343 | 1.28 (1.13–1.46) | 1.45 × 10−4 |
Adeno | 8p12 | rs4236709 | 32410110 | NRG1 | A_G | 0.225 | 1.10 (0.96–1.26) | 1.56 × 10−1 |
Adeno | 9p21.3 | rs885518 | 21830157 | MTAP/CDNK2A | A_G | 0.110 | 1.37 (1.16–1.62) | 2.20 × 10−4 |
Adeno | 10q24.3 | rs11591710 | 1.06E+08 | OBFC1 | A_C | 0.143 | 1.14 (0.97–1.33) | 1.21 × 10−1 |
Adeno | 11q23.3 | rs1056562 | 1.18E+08 | MPZL3/AMICA1 | C_T | 0.471 | 1.08 (0.96–1.21) | 1.89 × 10−1 |
Adeno | 15q21.1 | rs77468143 | 49376624 | SECISBP2L | T_G | 0.249 | 0.87 (0.76–0.99) | 4.00 × 10−2 |
Adeno | 20q13.33 | rs41309931 | 62326579 | RTEL1 | G_T | 0.119 | 1.35 (1.14–1.60) | 6.14 × 10−4 |
SQC | 6p21.33 | rs116822326 | 31434111 | MHC | A_G | 0.161 | 1.26 (1.03–1.54) | 2.36 × 10−2 |
SQC | 12p13.33 | rs7953330 | 998819 | RAD52 | G_C | 0.313 | 0.79 (0.66–0.94) | 7.05 × 10−3 |
SQC | 22q12.1 | rs17879961 | 29121087 | CHEK2 | A_G | 0.004 | 2.50 (0.76–8.15) | 1.29 × 10−1 |
EAF, effective allele frequency; OR, odds (log additive) ratio; 95% CI, 95% confidence interval; Adeno, adenocarcinoma; SQC, squamous cell carcinoma.
aDenotes reference_effect(coded) allele. Variants in bold are associated with familial lung cancer at nominal significance level of 0.05. Genome positions relative to GRCh37.