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. 2017 Jun 8;125(6):067002. doi: 10.1289/EHP347

Table 2.

Findings from the trans-ethnic, fixed-effects, inverse variance-weighted meta-analysis, including sub-threshold associations (5×108<p<5×106).

Chr Position Lead SNP CA /NCA Coded allele Frequency p-value Interaction Estimate (SE) n Nearest Gene SNPsa
Black Hispanic White
10 44,733,383 rs1619661 T/C 0.81 0.92 0.91 2.11×108 2.55 (0.46) 22,158 CXCL12 8
22 51,065,600 rs6151412 G/A 0.90 0.95 0.95 1.02×106 3.88 (0.79) 20,921 ARSA 1
8 83,252,586 rs10504754 A/G 0.74 0.47 0.43 1.53×108 1.54 (0.32) 22,158 SNX16 1
7 48,811,506 rs13309098 G/A 0.88 0.88 0.93 1.85×106 2.37 (0.50) 22,158 ABCA13-CDC14C 4
2 213,065,465 rs6725041 T/C 0.78 0.44 0.48 2.55×108 1.52 (0.32) 22,158 ERBB4 8
20 39,435,700 rs7361259 T/C 0.91     4.61×106 5.98 (1.39) 2,169 MAFB 1

Note: CA, coded allele; CAF, coded allele frequency; Chr, chromosome; NCA, noncoded allele; SE, standard error; SNP, single nucleotide polymorphism.

a

Total number of significant or sub-threshold SNPs located within the same gene or in LD with the lead SNP (r20.80).