ClinVar Miner

List of variants in gene MT-CO1 reported as uncertain significance by ClinGen Mitochondrial Disease Nuclear and Mitochondrial Variant Curation Expert Panel, ClinGen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CO1):m.6721T>C	rs199476127
NC_012920.1(MT-CO1):m.7092T>C	rs2124593818
m.6742T>C	rs199476126

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