RS201766777 WNK1
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Associated Conditions
Pseudohypoaldosteronism type 2C
Neuropathy
hereditary sensory and autonomic
type 2A
Inborn genetic diseases
Pseudohypoaldosteronism type 2C
Neuropathy
hereditary sensory and autonomic
type 2A
Inborn genetic diseases
Other Variants in WNK1