List of variants reported as uncertain significance for Coenzyme Q10 deficiency, primary, 3 by Fulgent Genetics, Fulgent Genetics

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_020381.4(PDSS2):c.667G>A (p.Val223Ile)	rs35555197	0.00130
NM_020381.4(PDSS2):c.1096C>T (p.Arg366Cys)	rs370257390	0.00006
NM_020381.4(PDSS2):c.50C>T (p.Ser17Leu)	rs373021095	0.00005
NM_020381.4(PDSS2):c.382G>A (p.Val128Met)	rs201645466	0.00003
NM_020381.4(PDSS2):c.488G>A (p.Arg163His)	rs142617068	0.00001
NM_020381.4(PDSS2):c.500A>G (p.Asn167Ser)	rs201218141	0.00001
NM_020381.4(PDSS2):c.1190_1191del (p.Arg397fs)	rs782439454

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