Table 1.
SNPa | Position on Chr. 13 (GRCh37) | Alleles (1 > 2)b | Risk Allele | Allele Frequency, % | P | Pcc | OR (95% CI)d | |
---|---|---|---|---|---|---|---|---|
Cases (N = 611) | Controls (N = 737) | |||||||
rs3825427 | 99,848,971 | C>A | A | 38.7 | 36.4 | 0.24 | 1.10 (0.94–1.29) | |
rs9513584 | 99,876,281 | G>A | G | 59.2 | 56.3 | 0.12 | 1.13 (0.97–1.32) | |
rs7999348 | 99,932,922 | G>A | G | 63.0 | 61.5 | 0.41 | 1.07 (0.91–1.25) | |
rs9517723 | 100,084,679 | T>C | T | 63.3 | 57.5 | 0.0024 | 0.13 | 1.27 (1.09–1.49) |
ars9513584, rs7999348, and rs9517723 were genotyped on the GWAS panel while rs3825427 was imputed with the 1000 Genomes reference panel. b1, major allele; 2, minor allele. c Pc, corrected P; If the Pc value is greater than 1, it is set to 1. dOR, odds ratio; CI, confidence interval.