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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WASHC5, WASHC5-AS1
(P770S +1 more)
Single nucleotide variant
(missense variant)
Spastic paraplegia
+3 more
GUncertain significance
WASHC5, WASHC5-AS1
(F734Y +1 more)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 8
GPathogenic