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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KAT6A
Deletion
(inframe_deletion)
not provided
+3 more
GBenign/Likely benign
KAT6A
(T1009M)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
KAT6A
(S448G)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
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