RS200557019 SCNN1A
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Associated Conditions
Inborn genetic diseases
Pseudohypoaldosteronism
type IB1
autosomal recessive
Liddle syndrome 3
Bronchiectasis with or without elevated sweat chloride 2
Inborn genetic diseases
Pseudohypoaldosteronism
type IB1
autosomal recessive
Liddle syndrome 3
Bronchiectasis with or without elevated sweat chloride 2
Other Variants in SCNN1A