ClinVar Miner

List of variants reported as uncertain significance for Coenzyme Q10 deficiency, primary, 1 by Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001358921.2(COQ2):c.533A>G (p.Asn178Ser)	rs121918232	0.00009
NM_001358921.2(COQ2):c.253+4A>T	rs907149421	0.00001

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