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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PYGM
(K754fs +1 more)
Deletion
(frameshift variant)
not provided
+1 more
GPathogenic/Likely pathogenic
PYGM
(R576* +1 more)
Single nucleotide variant
(nonsense)
Glycogen storage disease, type V
+1 more
GPathogenic/Likely pathogenic