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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP13A2
(P525L +1 more)
Single nucleotide variant
(missense variant)
Kufor-Rakeb syndrome
+1 more
GUncertain significance
ATP13A2
(T510M +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
ATP13A2
Single nucleotide variant
(splice donor variant)
Kufor-Rakeb syndrome
GLikely pathogenic
ATP13A2
Single nucleotide variant
(intron variant)
Autosomal recessive spastic paraplegia type 78
GUncertain significance
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