In contrast, the synonymous SNP rs3743123 (S196S) was nominally associated to the disease, at both allele (p = 0.03; OR = 1.27 [1.02–1.82]) and genotype levels, as assessed per a recessive model (p = 0.03; OR = 1.36 [1.02–1.59]), although this association did not reach statistical significance after correction for multiple testing ( S4 Table ).
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A Variant of GJD2, Encoding for Connexin 36, Alters the Function of Insulin Producing β-Cells.
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