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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP7B
(A874V +4 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
ATP7B
(R778L +2 more)
Single nucleotide variant
(missense variant +1 more)
ATP7B-related condition
+3 more
GPathogenic