List of variants reported as benign for Autosomal dominant mitochondrial myopathy with exercise intolerance

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_213720.3(CHCHD10):c.261+11A>G	rs131444	0.92009
NM_213720.3(CHCHD10):c.48A>C (p.Pro16=)	rs179468	0.91291
NM_213720.3(CHCHD10):c.312C>T (p.Tyr104=)	rs9153
NM_213720.3(CHCHD10):c.409+27G>C	rs140182

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