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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ATP7B
(H1069Q +4 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+2 more
GPathogenic
ATP7B
(R778L +2 more)
Single nucleotide variant
(missense variant +1 more)
ATP7B-related condition
+3 more
GPathogenic
ATP7B, LOC130009838
Deletion
(5 prime UTR variant +1 more)
Wilson disease
Gnot provided
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