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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130059818, SPG7
(G14fs)
Deletion
(frameshift variant)
Hereditary spastic paraplegia 7
GPathogenic
LOC130059818, SPG7
(W29*)
Single nucleotide variant
(nonsense)
Hereditary spastic paraplegia 7
GPathogenic