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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AP3B1
(V999M +1 more)
Single nucleotide variant
(missense variant)
Autoinflammatory syndrome
+4 more
GConflicting classifications of pathogenicity
AP3B1
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign/Likely benign