RS367681929 SCNN1A

Health Risk Chr 12:6347934
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Associated Conditions
Inborn genetic diseases
Pseudohypoaldosteronism
type IB1
autosomal recessive
Inborn genetic diseases
Pseudohypoaldosteronism
type IB1
autosomal recessive
Other Variants in SCNN1A
rs765835593 rs137852634 rs756434927 rs1592074026 rs137852635 rs61759860 rs149484264 rs146177203 rs62619209 rs199526819
Ask Dr. Hemsworth about this variant