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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AFG2B
(G176V)
Single nucleotide variant
(missense variant +1 more)
Neurodevelopmental delay
+4 more
GPathogenic/Likely pathogenic
AFG2B
(G689V)
Single nucleotide variant
(missense variant +1 more)
See cases
+3 more
GConflicting classifications of pathogenicity