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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AP4M1
(E193K +1 more)
Single nucleotide variant
(missense variant)
AP-4 deficiency syndrome
+1 more
GConflicting classifications of pathogenicity
AP4M1
Duplication
(inframe_insertion)
AP-4 deficiency syndrome
GUncertain significance