RS35731153 SCNN1B

Health Risk Chr 16:23348844
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Bronchiectasis with or without elevated sweat chloride 1
Liddle syndrome 1
Pseudohypoaldosteronism
type IB1
autosomal recessive
SCNN1B-related disorder
Bronchiectasis with or without elevated sweat chloride 1
Liddle syndrome 1
Pseudohypoaldosteronism
type IB1
autosomal recessive
SCNN1B-related disorder
Other Variants in SCNN1B
rs137852704 rs387906402 rs137852707 rs2142050610 rs137852708 rs137852709 rs1596894031 rs137852710 rs2303156 rs779990343
Ask Dr. Hemsworth about this variant