RS200966246 SCNN1B
Upload your DNA to see your genotype for this variant.
Associated Conditions
Bronchiectasis with or without elevated sweat chloride 1
Liddle syndrome 1
Pseudohypoaldosteronism
type IB1
autosomal recessive
Inborn genetic diseases
type IB2
Bronchiectasis with or without elevated sweat chloride 1
Liddle syndrome 1
Pseudohypoaldosteronism
type IB1
autosomal recessive
Inborn genetic diseases
type IB2
Other Variants in SCNN1B