ClinVar Miner

List of variants studied for Coenzyme Q10 deficiency, primary 1 by Broad Institute Rare Disease Group,Broad Institute

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Total variants: 2
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HGVS dbSNP
NM_001358921.2(COQ2):c.253+4A>T rs907149421
NM_015697.8(COQ2):c.683A>G (p.Asn228Ser) rs121918232

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