RS387906402 SCNN1B
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What This Variant Does
"CLNSIG=5
Associated Conditions
Liddle syndrome 1
Pseudohypoaldosteronism
type IB2
autosomal recessive
Bronchiectasis with or without elevated sweat chloride 1
Liddle syndrome 1
Liddle syndrome 1
Pseudohypoaldosteronism
type IB2
autosomal recessive
Bronchiectasis with or without elevated sweat chloride 1
Liddle syndrome 1
Other Variants in SCNN1B