RS148985177 SCNN1G

Health Risk Chr 16:23215108
Upload your DNA to see your genotype for this variant.
Associated Conditions
Liddle syndrome 2
Pseudohypoaldosteronism
type IB1
autosomal recessive
Bronchiectasis with or without elevated sweat chloride 3
SCNN1G-related disorder
type IB3
Liddle syndrome 2
Pseudohypoaldosteronism
type IB1
autosomal recessive
Bronchiectasis with or without elevated sweat chloride 3
SCNN1G-related disorder
type IB3
Other Variants in SCNN1G
rs137853342 rs1596779402 rs1567262640 rs1596779433 rs886041786 rs72647541 rs72646501 rs72647550 rs72647527 rs762522517
Ask Dr. Hemsworth about this variant