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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EEF2
(M494L)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 26
GUncertain significance
EEF2
(D295V)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 19/22
GUncertain significance