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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBCD
(G419R)
Single nucleotide variant
(missense variant)
Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome
GUncertain significance
TBCD
(E769del)
Microsatellite
(inframe_deletion)
Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome
GUncertain significance