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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VPS13D
(S4092* +1 more)
Single nucleotide variant
(nonsense)
Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome
GPathogenic
VPS13D
(G4152D +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome
GLikely pathogenic