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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP7B
(T974M +4 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
ATP7B
(Q260fs)
Duplication
(frameshift variant)
not provided
+1 more
GPathogenic/Likely pathogenic
ATP7B
(K175fs)
Deletion
(frameshift variant)
not provided
+2 more
GPathogenic/Likely pathogenic
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