ClinVar for MedGen (Select 1648371) - ClinVar - NCBI

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Items: 3

VariationLocation		Gene(s)	Protein change	Condition(s)	Clinical significance (Last reviewed)	Review status
Select item 97151.	m.10197G>A GRCh37: ChrMT:10197 GRCh38: ChrMT:10197	MT-ND3		Mitochondrial disease	Pathogenic (Jul 25, 2022)	reviewed by expert panel FDA Recognized Database
Select item 97142.	m.10158T>C GRCh37: ChrMT:10158 GRCh38: ChrMT:10158	MT-ND3		Mitochondrial disease	Pathogenic (Oct 26, 2021)	reviewed by expert panel FDA Recognized Database
Select item 97123.	m.10191T>C GRCh37: ChrMT:10191 GRCh38: ChrMT:10191	MT-ND3		Mitochondrial disease	Pathogenic (Aug 23, 2022)	reviewed by expert panel FDA Recognized Database