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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POLG
(R1096C)
Single nucleotide variant
(missense variant)
Mitochondrial disease
GLikely pathogenic
POLG
(R1047W)
Single nucleotide variant
(missense variant)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1
+5 more
GConflicting classifications of pathogenicity
POLG
(R964C)
Single nucleotide variant
(missense variant)
Mitochondrial DNA depletion syndrome 4b
+8 more
GConflicting classifications of pathogenicity
POLG
(P587L)
Single nucleotide variant
(missense variant)
Mitochondrial disease
+15 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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