Barely Significant
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Current limitations of SNP data from the public domain for studies of complex disorders: a test for ten candidate genes for obesity and osteoporosis.

BMC Genet · 2004 · PMC395827 · PMID 15113403

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nearly significantno p-value reported
Three more SNPs (SNP32, SNP33, and SNP41) manifested nearly significant differences in allele frequencies between these ethnic groups (Table 4 ).

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