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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AP4S1
(E51G)
Single nucleotide variant
(missense variant)
Spastic paraplegia 52, autosomal recessive
GUncertain significance
AP4S1
(R97*)
Single nucleotide variant
(nonsense)
Spastic paraplegia
+3 more
GPathogenic/Likely pathogenic