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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PYGM
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GLikely benign
PYGM
(M1V)
Single nucleotide variant
(missense variant +1 more)
Glycogen storage disease, type V
GPathogenic/Likely pathogenic