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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VPS13D
(E623G)
Single nucleotide variant
(missense variant)
Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome
GUncertain significance
VPS13D
(D3495Y +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance