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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DNA2
(A740G)
Single nucleotide variant
(missense variant +1 more)
Mitochondrial DNA deletion syndrome with progressive myopathy
GUncertain significance
DNA2
(R719I)
Single nucleotide variant
(missense variant +1 more)
Seckel syndrome 8
GUncertain significance
DNA2
(M236T)
Single nucleotide variant
(missense variant +1 more)
Seckel syndrome 8
GUncertain significance
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