RS574069625 WNK1
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Associated Conditions
Inborn genetic diseases
Neuropathy
hereditary sensory and autonomic
type 2A
Pseudohypoaldosteronism type 2C
Inborn genetic diseases
Neuropathy
hereditary sensory and autonomic
type 2A
Pseudohypoaldosteronism type 2C
Other Variants in WNK1