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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALS2
(R1341H)
Single nucleotide variant
(missense variant)
Infantile-onset ascending hereditary spastic paralysis
+2 more
GUncertain significance
ALS2
(T827S)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia
+5 more
GConflicting classifications of pathogenicity