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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP13A2
(E785K +1 more)
Single nucleotide variant
(missense variant)
Kufor-Rakeb syndrome
+2 more
GUncertain significance
ATP13A2
Single nucleotide variant
(splice donor variant)
Kufor-Rakeb syndrome
GUncertain significance
ATP13A2
(G504R +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive spastic paraplegia type 78
+2 more
GConflicting classifications of pathogenicity
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