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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VPS13D
(Q3951fs +1 more)
Deletion
(frameshift variant)
Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome
GPathogenic
VPS13D
(V4056A +1 more)
Single nucleotide variant
(missense variant)
Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome
GLikely pathogenic