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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MECR
(R258W +4 more)
Single nucleotide variant
(missense variant +1 more)
Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities
+1 more
GPathogenic
MECR
(N111fs +4 more)
Deletion
(frameshift variant +1 more)
Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities
+1 more
GPathogenic