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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SPG11
(T2033fs +1 more)
Microsatellite
(frameshift variant)
Hereditary spastic paraplegia 11
GPathogenic/Likely pathogenic
SPG11
(E1618*)
Single nucleotide variant
(nonsense)
Hereditary spastic paraplegia 11
GLikely pathogenic
SPG11
(F626fs)
Deletion
(frameshift variant)
Hereditary spastic paraplegia 11
GLikely pathogenic
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