RS200979623 WNK1
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Associated Conditions
Neuropathy
hereditary sensory and autonomic
type 2A
Pseudohypoaldosteronism type 2C
Inborn genetic diseases
Neuropathy
hereditary sensory and autonomic
type 2A
Pseudohypoaldosteronism type 2C
Inborn genetic diseases
Other Variants in WNK1