List of variants in gene MT-TH reported as uncertain significance for MELAS syndrome

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: 12

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TH):m.12143T>C	rs1603223568
NC_012920.1(MT-TH):m.12144A>G	rs1603223569
NC_012920.1(MT-TH):m.12150T>C	rs1603223574
NC_012920.1(MT-TH):m.12163A>G	rs1603223581
NC_012920.1(MT-TH):m.12173T>A	rs1556424075
NC_012920.1(MT-TH):m.12176G>A	rs1603223594
NC_012920.1(MT-TH):m.12184A>G	rs1603223603
NC_012920.1(MT-TH):m.12185G>A	rs1603223607
NC_012920.1(MT-TH):m.12201T>C	rs387906733
NC_012920.1(MT-TH):m.12202T>C	rs1603223613
NC_012920.1(MT-TH):m.12204A>C	rs1603223614
NC_012920.1(MT-TH):m.12205C>T	rs1603223615

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