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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATL1
(L192F)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 3A
GLikely pathogenic
ATL1
(R495W)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia
+3 more
GPathogenic/Likely pathogenic