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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP2B3
(V793M +1 more)
Single nucleotide variant
(missense variant)
X-linked progressive cerebellar ataxia
GUncertain significance
ATP2B3
(N1183Y)
Single nucleotide variant
(missense variant +1 more)
X-linked progressive cerebellar ataxia
GUncertain significance