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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MILR1, POLG2
(A482S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
MILR1, POLG2
(Q250R)
Single nucleotide variant
(missense variant)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4
GUncertain significance
MILR1, POLG2
(S248L)
Single nucleotide variant
(missense variant)
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4
+2 more
GUncertain significance
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