ClinVar Miner

List of variants reported as likely pathogenic for Mitochondrial complex III deficiency nuclear type 8 by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_181705.4(LYRM7):c.2T>C (p.Met1Thr)	rs531275086	0.00002

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