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

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Total variants: 13

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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.1046G>A (p.Arg349Gln)	rs201388841	0.00027
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.700A>G (p.Lys234Glu)	rs372737420	0.00001
NM_020381.4(PDSS2):c.1070G>T (p.Gly357Val)
NM_020381.4(PDSS2):c.1151C>A (p.Ala384Asp)	rs1236270228
NM_020381.4(PDSS2):c.1190_1191del (p.Arg397fs)	rs782439454
NM_020381.4(PDSS2):c.740G>A (p.Trp247Ter)
NM_020381.4(PDSS2):c.837G>A (p.Met279Ile)	rs753476156

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