List of variants reported as likely benign for Autosomal recessive ataxia due to ubiquinone deficiency by Fulgent Genetics, Fulgent Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_020247.5(COQ8A):c.1053C>T (p.Gly351=)	rs55958233	0.01103
NM_020247.5(COQ8A):c.1824C>T (p.Ser608=)	rs141270350	0.00152
NM_020247.5(COQ8A):c.1797C>T (p.Leu599=)	rs139551241	0.00070
NM_020247.5(COQ8A):c.1554C>T (p.Phe518=)	rs747135135	0.00005

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