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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COG8
(I548T +2 more)
Single nucleotide variant
(missense variant +1 more)
COG8-congenital disorder of glycosylation
GUncertain significance
COG8
(E296del)
Deletion
(inframe_deletion)
COG8-congenital disorder of glycosylation
GUncertain significance