List of variants reported as uncertain significance for Mitochondrial disease by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_002693.3(POLG):c.1402A>G (p.Asn468Asp)	rs145843073	0.00063
NM_002693.3(POLG):c.391T>C (p.Tyr131His)	rs562847013	0.00027
NC_012920.1(MT-TL2):m.12278T>C	rs1603223646
NM_002693.3(POLG):c.1384T>C (p.Ser462Pro)
NM_002693.3(POLG):c.3395G>A (p.Ser1132Asn)

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