RS201873521 SCNN1A

Health Risk Chr 12:6349331
Upload your DNA to see your genotype for this variant.
Associated Conditions
Liddle syndrome 3
Pseudohypoaldosteronism
type IB1
autosomal recessive
Bronchiectasis with or without elevated sweat chloride 2
Liddle syndrome 3
Pseudohypoaldosteronism
type IB1
autosomal recessive
Bronchiectasis with or without elevated sweat chloride 2
Other Variants in SCNN1A
rs765835593 rs137852634 rs756434927 rs1592074026 rs137852635 rs61759860 rs149484264 rs146177203 rs62619209 rs199526819
Ask Dr. Hemsworth about this variant