RS398122838 FBXO38
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neuronopathy
distal hereditary motor
type 2D
Distal hereditary motor neuropathy type 2
Neuronopathy
distal hereditary motor
type 2D
Distal hereditary motor neuropathy type 2
Other Variants in FBXO38