ClinVar Miner

List of variants in gene SCNN1G reported as uncertain significance for Pseudohypoaldosteronism type 1 autosomal recessive; Bronchiectasis with or without elevated sweat chloride 3; LIDDLE SYNDROME 2

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Total variants: 1
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NM_001039.4(SCNN1G):c.1550T>C (p.Met517Thr) rs144653364

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