RS56153525 SCNN1G

Health Risk Chr 16:23215797
Upload your DNA to see your genotype for this variant.
Associated Conditions
Liddle syndrome 2
Pseudohypoaldosteronism
type IB1
autosomal recessive
Liddle syndrome 2
Pseudohypoaldosteronism
type IB1
autosomal recessive
Other Variants in SCNN1G
rs137853342 rs1596779402 rs1567262640 rs1596779433 rs886041786 rs72647541 rs72646501 rs148985177 rs72647550 rs72647527
Ask Dr. Hemsworth about this variant