List of variants in gene MT-TC 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: 6

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TC):m.5791G>A	rs1603220121
NC_012920.1(MT-TC):m.5793A>G	rs1603220122
NC_012920.1(MT-TC):m.5802T>C	rs1603220128
NC_012920.1(MT-TC):m.5804A>G	rs1603220130
NC_012920.1(MT-TC):m.5809G>A	rs1603220134
NC_012920.1(MT-TC):m.5819T>C	rs1603220139

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