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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GEMIN5
(Y1498* +1 more)
Duplication
(nonsense)
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction
GConflicting classifications of pathogenicity
GEMIN5
(R1013W +1 more)
Single nucleotide variant
(missense variant)
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction
GUncertain significance