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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCT5
Deletion
(intron variant)
Hereditary sensory and autonomic neuropathy with spastic paraplegia
GConflicting classifications of pathogenicity
CCT5
(T129S +4 more)
Single nucleotide variant
(missense variant)
Hereditary sensory and autonomic neuropathy with spastic paraplegia
GUncertain significance