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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GLDC
(F334L)
Single nucleotide variant
(missense variant)
Glycine encephalopathy 1
+5 more
GUncertain significance
GLDC
(T269M)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic/Likely pathogenic