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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GOT1
Single nucleotide variant
(intron variant)
not provided
GBenign/Likely benign
GOT1
(E183G)
Single nucleotide variant
(missense variant)
not provided
GBenign
CPN1, CRTAC1
+95 more
Duplication
not provided
GUncertain significance
ABCC2, CNNM1
+8 more
Deletion
not provided
GPathogenic
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