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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALS2
(E702*)
Single nucleotide variant
(nonsense)
Juvenile primary lateral sclerosis
+2 more
GLikely pathogenic
ALS2
(R201*)
Single nucleotide variant
(nonsense)
Infantile-onset ascending hereditary spastic paralysis
+2 more
GPathogenic/Likely pathogenic