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. 2014 Jul 24;23(23):6407–6418. doi: 10.1093/hmg/ddu346

Table 3.

Meta-analysis results for PC2

SNP Allele 1 Allele 2 Z-score P-value Direction Chr Position Gene Feature Left gene Right gene
rs681524 t c −5.505 3.69E-08 ?------- 11 116253524 SIK3 intron APOA1 LOC100129905
rs1393902 a g 5.119 3.07E-07 ++++++++ 8 68584119 CPA6 intron ARFGEF1 LOC100132812
rs1503369 t c 5.116 3.12E-07 ++++++++ 8 68584552 CPA6 intron ARFGEF1 LOC100132812
rs1827524 a g 5.104 3.32E-07 ++++++-+ 8 68587796 CPA6 intron ARFGEF1 LOC100132812
rs1393901 t c 5.100 3.40E-07 ++++++-+ 8 68587888 CPA6 intron ARFGEF1 LOC100132812
rs6472312 t g −4.994 5.92E-07 ------+- 8 68572052 CPA6 intron ARFGEF1 LOC100132812
rs1503363 a g −4.940 7.80E-07 ------+- 8 68569258 CPA6 intron ARFGEF1 LOC100132812

Seven SNPs were suggestive genome-wide significant (P < 5 × 10−7) associated with PC2. Top associated SNPs for PC2 are further characterized by corresponding non-effect allele (allele 1) and effect allele (allele 2), the resulting Z-score and significance of association (P-value). The direction of effect (minus or plus) is indicated for each of the eight included populations. If an SNP did not pass QC criteria for a certain SNP, this is indicated by a question mark (?) in the direction column. Mapping information for each SNP is specified by chromosome (chr), base-pair position (position), genes at this locus (gene) and surrounding the locus (left and right gene) as well as feature of the SNP position within a gene (feature).