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  • Molecular assay reagents intended to identify mutations in the sodium channel epithelial 1 beta subunit (SCNN1B) gene, located at chromosome 16p12.2, which encodes the protein amiloride-sensitive sodium channel subunit beta. Genetic variants at this locus have been associated with bronchiectasis, pseudohypoaldosteronism, and pseudoprimary hyperaldosteronism.
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