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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP7B
(A874V +4 more)
Single nucleotide variant
(missense variant)
Wilson disease
+1 more
GPathogenic/Likely pathogenic
ATP7B
(A784V +2 more)
Single nucleotide variant
(missense variant +1 more)
Wilson disease
GPathogenic
ATP7B
(R778L +2 more)
Single nucleotide variant
(missense variant +1 more)
Wilson disease
+3 more
GPathogenic
ATP7B
Single nucleotide variant
(splice donor variant +1 more)
Wilson disease
+2 more
GPathogenic
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