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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CPT2
Single nucleotide variant
(synonymous variant +1 more)
Encephalopathy, acute, infection-induced, susceptibility to, 4
+6 more
GBenign/Likely benign
CPT2
Single nucleotide variant
(synonymous variant +1 more)
CPT2-related disorder
+2 more
GConflicting classifications of pathogenicity
CPT2
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GConflicting classifications of pathogenicity
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