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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AGL
(T38S +1 more)
Single nucleotide variant
(missense variant)
Glycogen storage disease type III
GUncertain significance
AGL
(W1451C +6 more)
Single nucleotide variant
(missense variant)
Glycogen storage disease type III
GPathogenic/Likely pathogenic