RS61729789 SCNN1B
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Associated Conditions
Liddle syndrome 1
Pseudohypoaldosteronism
type IB1
autosomal recessive
Bronchiectasis with or without elevated sweat chloride 1
Inborn genetic diseases
Inborn genetic diseases
Liddle syndrome 1
Pseudohypoaldosteronism
type IB1
autosomal recessive
Bronchiectasis with or without elevated sweat chloride 1
Inborn genetic diseases
Inborn genetic diseases
Other Variants in SCNN1B