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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FBXO38
(C206R)
Single nucleotide variant
(missense variant)
Distal hereditary motor neuropathy type 2
GPathogenic
FBXO38
(P739T)
Single nucleotide variant
(missense variant +1 more)
Neuronopathy, distal hereditary motor, type 2D
GPathogenic