Table 2.
SNP | Gene/locus | Allelea | Risk allele Frequency (%) |
HetOR (95 % CI) | P value | HomOR (95 % CI) | P value | Per risk allele (95 % CI) | P value | |
---|---|---|---|---|---|---|---|---|---|---|
Case | Control | |||||||||
rs1219648 | FGFR2 | A/G | 45.7 | 38.2 | 1.60 (1.19–2.16) | 0.001 | 1.70 (1.15–2.51) | 0.004 | 1.36 (1.13–1.65) | 0.001 |
rs2981582 | FGFR2 | G/A | 50.2 | 39.4 | 2.00 (1.47–2.73) | 0.000004 | 2.23 (1.51–3.29) | 0.00001 | 1.55 (1.28–1.88) | 0.000003 |
rs8051542 | TNRC9b | C/T | 44.5 | 36.4 | 1.15 (0.86–1.54) | 0.32 | 2.11 (1.39–3.19) | 0.0001 | 1.40 (1.16–1.69) | 0.0004 |
rs12443621 | TNRC9 | G/A | 46.6 | 48.2 | 0.86 (0.63–1.18) | 0.34 | 0.89 (0.61–1.30) | 0.53 | 0.94 (0.78–1.13) | 0.49 |
rs3803662 | TNRC9 | C/T | 45.9 | 43.5 | 1.12 (0.83–1.52) | 0.45 | 1.19 (0.82–1.72) | 0.34 | 1.10 (0.91–1.33) | 0.3 |
rs889312 | MAP3K1 | A/C | 35.1 | 28.9 | 1.37 (1.03–1.81) | 0.02 | 1.74 (1.08–2.82) | 0.01 | 1.33 (1.09–1.63) | 0.003 |
rs3817198 | LSP1 | T/C | 32.1 | 28.4 | 1.15 (0.87–1.52) | 0.3 | 1.45 (0.90–2.34) | 0.1 | 1.19 (0.97–1.46) | 0.08 |
rs13387042 | 2q35 | A/G | 41.6 | 44.8 | 0.92 (0.68–1.25) | 0.5 | 0.76 (0.52–1.12) | 0.15 | 0.88 (0.73–1.06) | 0.16 |
rs13281615 | 8q24 | A/G | 55.2 | 50.4 | 1.19 (0.85–1.66) | 0.3 | 1.44 (0.99–2.10) | 0.04 | 1.21 (1.00–1.46) | 0.03 |
CI confidence interval, OR odds ratio, HetOR odds ratio in heterozygote, HomOR odds ratio in homozygote for risk allele (relative to homozygote for non-risk allele)
aReference allele/risk allele
bAlso known as TOX3