RS137852704 SCNN1B

Health Risk Chr 16:23380574
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What This Variant Does
"[OMIM:?]
Associated Conditions
Liddle syndrome 1
Bronchiectasis with or without elevated sweat chloride 1
Pseudohypoaldosteronism
type IB2
autosomal recessive
Liddle syndrome 1
Bronchiectasis with or without elevated sweat chloride 1
Pseudohypoaldosteronism
type IB2
autosomal recessive
Other Variants in SCNN1B
rs387906402 rs137852707 rs2142050610 rs137852708 rs137852709 rs1596894031 rs137852710 rs35731153 rs2303156 rs779990343
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