Table 3.
Top SNPs from Cumulative Dose to Event Analysis
| SNP | Chr | Genea | Alleles | Discovery (n=855) |
European Replication (n=154)d |
African American Replication (n=117) |
||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| MAF b | HR (95% CI) |
Pc | MAF | HR (95% CI) |
P | MAF | HR (95% CI) |
P | ||||
| rs7349683 | 4 | EPHA5 | C/T | 0.36 | 1.63 (1.34–1.98) |
9.6 × 10−7 | 0.32 | 0.96 (0.57–1.60) |
0.43 | 0.13 | 1.16 (0.55–2.42) |
0.35 |
| rs4737264 | 8 | XKR4 | A/C | 0.22 | 1.68 (1.36–2.09) |
1.9×10−6 | 0.24 | 1.84 (1.02–3.33) |
0.021 | 0.18 | 1.23 (0.69–2.21) |
0.24 |
| rs10771973 | 12 | FGD4 | G/A | 0.31 | 1.57 (1.30–1.91) |
2.6 × 10−6 | 0.33 | 1.72 (1.06–2.80) |
0.013 | 0.17 | 1.93 (1.13–3.28) |
6.7 × 10−3 |
| rs16948748 | 17 | PITPNA | T/G | 0.04 | 2.37 (1.63–3.44) |
2.7 × 10−6 | 0.02 | 2.65e (0.63–11.1) |
0.083 | 0.07 | 1.07e (0.41–2.77) |
0.45 |
| rs16916932 | 10 | CACNB2 | C/T | 0.06 | 2.08 (1.51–2.87) |
4.3 × 10−6 | 0.06 | 0.38e (0.09–1.58) |
0.082 | 0.08 | 1.13e (0.47–2.74) |
0.39 |
| rs17781082 | 12 |
GRIP1/ CAND1 |
C/T | 0.42 | 1.60 (1.31–1.96) |
4.3 × 10−6 | 0.43 | 1.22 (0.74–1.99) |
0.22 | 0.21 | 1.32 (0.76–2.30) |
0.16 |
| rs1903216 | 3 | BCL6/ | G/A | 0.48 | 1.59 (1.30–1.95) |
5.6 × 10−6 | 0.41 | 2.08f (0.99–4.37) |
0.024 | 0.03 | 3.02f (1.04–8.73) |
0.016 |
| rs2233335 | 8 | NDRG1 | T/G | 0.38 | 0.65 (0.52–0.80) |
5.2 × 10−5 | 0.39 | 0.94 (0.58–1.53) |
0.41 | 0.23 | 1.40 (075–2.60) |
0.14 |
Intergenic SNPs are denoted by the closest flanking annotated gene(s).
Minor allele frequency (MAF) was calculated within the indicated cohort.
P-values are two-sided for discovery analysis and one-sided for replication.
As stated in the replication plan, analyses were exploratory for all except the EPHA5 and FGD4 SNPs.
Analysis assumed a dominant model.
Analysis assumed a recessive model.