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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACTL6B
(G343R)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability
+4 more
GPathogenic/Likely pathogenic
ACTL6B
(R97*)
Single nucleotide variant
(nonsense +1 more)
Developmental and epileptic encephalopathy, 76
+1 more
GLikely pathogenic
ACTL6B
(D77G)
Single nucleotide variant
(missense variant +1 more)
Intellectual developmental disorder with severe speech and ambulation defects
GUncertain significance
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