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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WNK1
(M214fs)
Deletion
(frameshift variant)
Neuropathy, hereditary sensory and autonomic, type 2A
+1 more
GConflicting classifications of pathogenicity
WNK1
(G307fs)
Insertion
(frameshift variant)
Charcot-Marie-Tooth disease
GUncertain significance
WNK1
(F356fs)
Deletion
(frameshift variant)
Charcot-Marie-Tooth disease
GUncertain significance
WNK1
(V364fs)
Insertion
(frameshift variant)
Charcot-Marie-Tooth disease
GUncertain significance
WNK1
(A380fs)
Duplication
(frameshift variant)
Charcot-Marie-Tooth disease
GUncertain significance
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