List of variants in gene MT-ATP6 reported as not provided

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: 22

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-ATP6):m.8636T>C	rs2124594840
NC_012920.1(MT-ATP6):m.8723G>T
NC_012920.1(MT-ATP6):m.8806C>T	rs2068712160
NC_012920.1(MT-ATP6):m.8821T>A	rs1603221825
NC_012920.1(MT-ATP6):m.8878C>T	rs2068712730
NC_012920.1(MT-ATP6):m.8946A>T	rs879181854
NC_012920.1(MT-ATP6):m.8975T>C	rs1981459
NC_012920.1(MT-ATP6):m.9155A>G
NC_012920.1:m.8651T>C	rs1556423512
NC_012920.1:m.8686T>C	rs1569484231
NC_012920.1:m.8839G>C	rs1556423547
NC_012920.1:m.8851T>C	rs199476136
NC_012920.1:m.8989G>C	rs587776444
NC_012920.1:m.8993T>C	rs199476133
NC_012920.1:m.9041A>G	rs879244322
NC_012920.1:m.9152T>C	rs878853096
NC_012920.1:m.9157G>A	rs1556423625
NC_012920.1:m.9176T>C	rs199476135
NC_012920.1:m.9176T>G	rs199476135
NC_012920.1:m.9185T>C	rs199476138
NC_012920.1:m.9191T>C	rs1556423632
m.9101T>C	rs199476134

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