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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GAA
Single nucleotide variant
(intron variant)
Glycogen storage disease, type II
GPathogenic
GAA
(R89H)
Single nucleotide variant
(missense variant)
Glycogen storage disease, type II
GUncertain significance
GAA
(M318T)
Single nucleotide variant
(missense variant)
Glycogen storage disease, type II
GPathogenic
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