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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SCN2A
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely pathogenic
ATP1A3
(L878fs +2 more)
Duplication
(frameshift variant)
Dystonia 12
GLikely pathogenic