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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AFG2B
(G32D)
Single nucleotide variant
(missense variant +1 more)
Neurodevelopmental disorder with hearing loss and spasticity
GUncertain significance
AFG2B
(G176V)
Single nucleotide variant
(missense variant +1 more)
not provided
+5 more
GPathogenic/Likely pathogenic