RS111033590 WNK1

Health Risk Chr 12:868772
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What This Variant Does
"[OMIM:?]
Associated Conditions
Neuropathy
hereditary sensory and autonomic
type 2A
Inborn genetic diseases
Pseudohypoaldosteronism type 2C
Neuropathy
hereditary sensory and autonomic
type 2A
Inborn genetic diseases
Pseudohypoaldosteronism type 2C
Other Variants in WNK1
rs111033592 rs111033591 rs387906331 rs387906332 rs137852734 rs137852735 rs786205473 rs72650720 rs201995891 rs72650768
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