RS139012605 SCNN1G

Health Risk Chr 16:23215380
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Associated Conditions
Liddle syndrome 2
Pseudohypoaldosteronism
type IB1
autosomal recessive
Inborn genetic diseases
Monosomy 7 myelodysplasia and leukemia syndrome 1
Liddle syndrome 2
Pseudohypoaldosteronism
type IB1
autosomal recessive
Inborn genetic diseases
Monosomy 7 myelodysplasia and leukemia syndrome 1
Other Variants in SCNN1G
rs137853342 rs1596779402 rs1567262640 rs1596779433 rs886041786 rs72647541 rs72646501 rs148985177 rs72647550 rs72647527
Ask Dr. Hemsworth about this variant