RS137852635 SCNN1A

Health Risk Chr 12:6348198
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Pseudohypoaldosteronism
type IB1
autosomal recessive
Pseudohypoaldosteronism
type IB1
autosomal recessive
Other Variants in SCNN1A
rs765835593 rs137852634 rs756434927 rs1592074026 rs61759860 rs149484264 rs146177203 rs62619209 rs199526819 rs72657550
Ask Dr. Hemsworth about this variant