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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TGM6
(R378fs)
Duplication
(frameshift variant)
Spinocerebellar ataxia type 35
GUncertain significance
TGM6
(G388D)
Single nucleotide variant
(missense variant)
Spinocerebellar ataxia type 35
GUncertain significance