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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POLG
(R1142Q)
Single nucleotide variant
(missense variant)
not provided
+6 more
GUncertain significance
POLG
(R1047W)
Single nucleotide variant
(missense variant)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1
+5 more
GConflicting classifications of pathogenicity
POLG
(T251I)
Single nucleotide variant
(missense variant)
POLG-Related Spectrum Disorders
+16 more
GConflicting classifications of pathogenicity
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