ClinVar for MedGen (Select 865038) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 9665	m.6721T>C	MT-CO1	Single nucleotide variant	Myelodysplastic syndrome with ring sideroblasts	GPathogenic
Select item 9664	m.6742T>C	MT-CO1	Single nucleotide variant	Mitochondrial disease	GUncertain significance FDA Recognized database