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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POLG, POLGARF
(R1142Q)
Single nucleotide variant
(missense variant)
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
+6 more
GUncertain significance
POLG, POLGARF
(R1047W)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+5 more
GConflicting classifications of pathogenicity
POLG, POLGARF
(T251I)
Single nucleotide variant
(missense variant)
not specified
+15 more
GConflicting classifications of pathogenicity
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