ClinVar Miner

List of variants reported as likely pathogenic for Inborn mitochondrial myopathy by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_018116.4(MSTO1):c.706G>C (p.Asp236His)	rs753488873	0.00013
NM_018116.4(MSTO1):c.651C>G (p.Phe217Leu)	rs776826330	0.00012

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