Barely Significant
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Fine-Mapping of 18q21.1 Locus Identifies Single Nucleotide Polymorphisms Associated with Nonsyndromic Cleft Lip with or without Cleft Palate.

Front Genet · 2016 · PMC4876112 · PMID 27242896

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highly significantno p-value reported
In our study, SKA1 SNP rs6507992 showed highly significant association with the NSCL/P phenotype, rs6507992 GG had an odds ratio of 15.41 compared to the rs6507992 AA and GA genotypes combined (OR AA+GA vs.

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