ClinVar Miner

List of variants reported as likely pathogenic for Mitochondrial disease by Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet

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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_017446.4(MRPL39):c.896G>T (p.Gly299Val)	rs1227035820

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