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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POLG
(G848S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+11 more
GPathogenic
POLG
(A467T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+12 more
GPathogenic