List of variants in gene MT-ATP6 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: 7

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ATP6):m.8803A>T	rs878853020
NC_012920.1(MT-ATP6):m.8851T>C	rs199476136
NC_012920.1(MT-ATP6):m.8936T>A	rs1603221920
NC_012920.1(MT-ATP6):m.9026G>A	rs1603221987
NC_012920.1(MT-ATP6):m.9032T>C	rs1603221994
NC_012920.1(MT-ATP6):m.9038T>C	rs1603222003
NC_012920.1(MT-ATP6):m.9152T>C	rs878853096

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