RS137852634 SCNN1A

Health Risk Chr 12:6348981
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What This Variant Does
"[OMIM:?]
Associated Conditions
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
Liddle syndrome 3
Other Variants in SCNN1A
rs765835593 rs756434927 rs1592074026 rs137852635 rs61759860 rs149484264 rs146177203 rs62619209 rs199526819 rs72657550
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