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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MGME1
(R220Q +2 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+2 more
GUncertain significance
MGME1
(T222N +3 more)
Single nucleotide variant
(missense variant)
Mitochondrial DNA depletion syndrome 11
GUncertain significance