List of variants in gene MT-ATP6 reported 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
		ClinVar version:

Total variants: 18

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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.8932C>T	rs878853013
NC_012920.1(MT-ATP6):m.8936T>A	rs1603221920
NC_012920.1(MT-ATP6):m.8969G>A	rs794726857
NC_012920.1(MT-ATP6):m.8993T>C	rs199476133
NC_012920.1(MT-ATP6):m.9026G>A	rs1603221987
NC_012920.1(MT-ATP6):m.9032T>C	rs1603221994
NC_012920.1(MT-ATP6):m.9035T>C	rs1603222000
NC_012920.1(MT-ATP6):m.9038T>C	rs1603222003
NC_012920.1(MT-ATP6):m.9055G>A	rs193303045
NC_012920.1(MT-ATP6):m.9091A>G	rs1057520079
NC_012920.1(MT-ATP6):m.9152T>C	rs878853096
NC_012920.1(MT-ATP6):m.9155A>G
NC_012920.1(MT-ATP6):m.9176T>C	rs199476135
NC_012920.1(MT-ATP6):m.9176T>G	rs199476135
NC_012920.1(MT-ATP6):m.9185T>C	rs199476138
NC_012920.1(MT-ATP6):m.9191T>C	rs1556423632

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