RS2506496921 SCNN1B

Health Risk Chr 16:23377241
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Associated Conditions
Pseudohypoaldosteronism
type IB2
autosomal recessive
Pseudohypoaldosteronism
type IB2
autosomal recessive
Other Variants in SCNN1B
rs137852704 rs387906402 rs137852707 rs2142050610 rs137852708 rs137852709 rs1596894031 rs137852710 rs35731153 rs2303156
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