List of variants reported as benign for Autosomal recessive ataxia due to ubiquinone deficiency by Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_020247.5(COQ8A):c.1660-9T>C	rs7552783	0.45219
NM_020247.5(COQ8A):c.1716T>C (p.Ser572=)	rs3738725	0.42035
NM_020247.5(COQ8A):c.117G>A (p.Ala39=)	rs11549708	0.16388
NM_020247.5(COQ8A):c.63G>A (p.Ala21=)	rs11549709	0.01280
NM_020247.5(COQ8A):c.1440C>T (p.Phe480=)	rs12593

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