Table 2.
Region | Candidate Gene(s) | Total SNPsa | MAFb |
No. of SNPs Identified |
||
---|---|---|---|---|---|---|
Bonferroni | BH | WBH | ||||
2p23.3 | GCKR | 1 | 0.40 | 0 | 0 | 1 |
2q24.3 | G6PC2, ABCB11 | 19 | 0.29 ∼0.48 | 17 | 18 | 19 |
4q31.23 | NR3C2 | 1 | 0.072 | 0 | 0 | 1 |
6p12.3 | RUNX2 | 1 | 0.28 | 0 | 0 | 1 |
7p13 | GCK | 4 | 0.17 ∼0.22 | 4 | 4 | 4 |
11q21 | MTNR1B | 8 | 0.28 ∼0.43 | 7 | 7 | 8 |
13q21.32 | PCDH9 | 1 | 0.00018 | 1 | 1 | 1 |
20p11.21 | FOXA2 | 1 | 0.042 | 0 | 0 | 1 |
Total | 36 | 29 | 30 | 36 |
The Bonferroni correction procedure controls the family-wise error rate at 0.05, whereas both the BH and WBH procedures control the FDR at 0.05. Abbreviations are as follows: MAF, minor allele frequency; BH, Benjamini and Hochberg procedure; WBH, weighted Benjamini and Hochberg procedure.
The number of significant SNPs in each region obtained with the use of the three procedures. The numbers are identical to those of the WBH procedure in this study.
The range of MAF for all of the significant SNPs (column 2) in each region calculated in the EA population of the ARIC.