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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130058947, PHKB
(E10D)
Single nucleotide variant
(missense variant +1 more)
Glycogen storage disease IXb
GConflicting classifications of pathogenicity
PHKB
(N625D +1 more)
Single nucleotide variant
(missense variant)
Glycogen storage disease IXb
GUncertain significance