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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HDAC4
(P248L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+4 more
GConflicting classifications of pathogenicity
HDAC4
(T244K)
Single nucleotide variant
(missense variant)
Intellectual disability, severe
+1 more
GPathogenic/Likely pathogenic