List of variants in gene MT-TF 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: 5

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.579T>C	rs1603218447
NC_012920.1(MT-CYB):m.588T>C	rs1603218449
NC_012920.1(MT-CYB):m.624C>T	rs1603218465
NC_012920.1(MT-CYB):m.628C>T	rs1603218467
NC_012920.1(MT-CYB):m.643A>G	rs1603218472

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