"Centogene AG - the Rare Disease Company"[submitter] AND "DNA2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1333770	NM_001080449.3(DNA2):c.2546G>T (p.Gly849Val)	DNA2 (G849V)	Single nucleotide variant (missense variant +1 more)	Mitochondrial DNA deletion syndrome with progressive myopathy	GUncertain significance
Select item 1333768	NM_001080449.3(DNA2):c.1450del (p.Arg484fs)	DNA2 (R484fs)	Deletion (frameshift variant +1 more)	Mitochondrial DNA deletion syndrome with progressive myopathy	GUncertain significance