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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC37A4
Deletion
(frameshift variant)
Glucose-6-phosphate transport defect
GConflicting classifications of pathogenicity
SLC37A4
(V198D +1 more)
Single nucleotide variant
(missense variant)
Glucose-6-phosphate transport defect
GUncertain significance