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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP13A2
(E362K +1 more)
Single nucleotide variant
(missense variant)
Kufor-Rakeb syndrome
+1 more
GConflicting classifications of pathogenicity
ATP13A2
(Q225* +1 more)
Single nucleotide variant
(nonsense)
Autosomal recessive spastic paraplegia type 78
GPathogenic