List of variants reported as likely benign for Mitochondrial DNA deletion syndrome with progressive myopathy; Seckel syndrome 8 by Fulgent Genetics, Fulgent Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001080449.3(DNA2):c.888G>A (p.Pro296=)	rs16925390	0.01237
NM_001080449.3(DNA2):c.1649A>G (p.Asn550Ser)	rs141731085	0.00726
NM_001080449.3(DNA2):c.295T>C (p.Leu99=)	rs140077857	0.00675
NM_001080449.3(DNA2):c.2430C>G (p.Phe810Leu)	rs73274785
NM_001080449.3(DNA2):c.720-4del	rs34191745

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