ClinVar Miner

List of variants in gene MT-ND6 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-ND6):m.14596A>T	rs387906424
NC_012920.1(MT-ND6):m.14598T>C	rs1057518882
NC_012920.1(MT-ND6):m.14633A>G	rs1569484667

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