ClinVar Miner

List of variants in gene MT-CO2 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-CO2):m.7637G>A	rs1556423314
NC_012920.1(MT-CO2):m.7724A>T	rs1553139599
NC_012920.1(MT-CO2):m.7746A>G	rs1603221113

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