RS111033591 WNK1
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What This Variant Does
"[OMIM:?]
Associated Conditions
Neuropathy
hereditary sensory and autonomic
type 2A
Pseudohypoaldosteronism type 2C
Hereditary neuropathy or pain disorder
Neuropathy
hereditary sensory and autonomic
type 2A
Pseudohypoaldosteronism type 2C
Hereditary neuropathy or pain disorder
Other Variants in WNK1