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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP2U1
(D316V)
Single nucleotide variant
(missense variant)
not provided
+2 more
GPathogenic/Likely pathogenic
CYP2U1
(G529D)
Single nucleotide variant
(missense variant)
Hereditary spastic paraplegia 56
GUncertain significance