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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ALG13
(E738G +3 more)
Single nucleotide variant
(missense variant +1 more)
Developmental and epileptic encephalopathy, 36
+1 more
GConflicting classifications of pathogenicity
ALG13
Single nucleotide variant
(splice acceptor variant)
not provided
+1 more
GUncertain significance
ALG13
Microsatellite
(inframe_deletion +1 more)
not specified
+2 more
GConflicting classifications of pathogenicity
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