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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EXOSC5
(M148T)
Single nucleotide variant
(missense variant)
Cerebellar ataxia, brain abnormalities, and cardiac conduction defects
+1 more
GUncertain significance
EXOSC5
Single nucleotide variant
(missense variant)
Cerebellar ataxia, brain abnormalities, and cardiac conduction defects
GPathogenic/Likely pathogenic
EXOSC5
Single nucleotide variant
(missense variant)
Cerebellar ataxia, brain abnormalities, and cardiac conduction defects
GPathogenic/Likely pathogenic
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