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. 2017 Dec 6;7:17075. doi: 10.1038/s41598-017-17136-0

Table 2.

Genome-wide significant secondary SNPs from previously reported regions, identified in meta-analyzed conditional analysis.

Locus SNP Chr Position (hg19) A1 A2 CAF β (ms) Direction of β SE (ms) P-val PHet
NOS1AP rs3934467 1 162,182,677 T C 0.28 1.62 ++++ 0.24 2.26e–11 0.78
rs73017364 1 162,184,746 T C 0.87 1.73 ++++ 0.31 3.74e–08 0.65
ATP1B1 rs1320977 1 169,073,388 A G 0.15 −2.30 −−−+ 0.29 2.61e–15 0.02
rs1138486 1 169,101,935 T C 0.14 −2.46 −−−? 0.31 6.98e–15 0.55
SCN5A rs6762565 3 38,582,191 T C 0.19 −1.65 ?−−? 0.29 1.94e–08 0.19
KCNQ1 rs78695585 11 2,644,544 A G 0.04 3.48 ++++ 0.59 2.82e–09 0.63

Chr: chromosome number. Position: the base pair position in Build 37 (hg19). A1, A2: coded/non-coded alleles. CAF: coded allele frequency. β: effect estimate in ms for the highest associated SNP upon conditional analysis. Direction: the direction of the effect estimates; order is WHI, MESA, HCHS/SOL, and Starr County; ‘?’ means the SNP was not present for a particular study. SE: standard error (ms). Phet: P-val for Cochran’s Q test of homogeneity among cohorts, for the highest associated SNP upon conditional analysis.