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. 2013 Aug 8;93(2):298–305. doi: 10.1016/j.ajhg.2013.05.026

Table 2.

Genetic Association Results of the Most Significant SNP, rs10919543, in the FCGR2A/FCGR3A Locus and All Genetic Variants in High LD with This SNP

SNP (Minor Allele) Turkish
European-American
Meta-analysis
MAFCase MAFControl OR 95% CI p MAFCase MAFControl OR 95% CI p OR pmeta Q Statistic p
rs10919543 (G) 0.559 0.413 1.80 (1.47–2.22) 1.49 × 10−8 0.462 0.320 1.82 (1.35–2.46) 6.71 × 10−5 1.81 5.89 × 10−12 0.952
rs10919544 (C) 0.560 0.413 1.81 (1.47–2.22) 1.50 × 10−8 0.458 0.325 1.75 (1.30–2.36) 0.0002012 1.79 1.61 × 10−11 0.874
rs2099684 (G) 0.554 0.415 1.75 (1.43–2.15) 7.17 × 10−8 0.458 0.323 1.77 (1.32–2.39) 0.0001497 1.76 5.70 × 10−11 0.951
rs141730227 (T) NA NA NA NA NA 0.462 0.324 1.79 (1.33–2.42) 0.000131 NA NA NA

NA: The SNP rs141730227 was not evaluated in the Turkish cohort because the genotype success rate (GSR) of 0.898 was below our GSR threshold for SNP inclusion. However, when analyzed, it did show evidence for association (OR = 1.735 [1.397–2.155], p = 5.754 × 10−7).