List of variants in gene MT-TI reported as uncertain significance for hereditary skeletal muscle disorder

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-TI):m.4264G>A	rs1603219385
NC_012920.1(MT-TI):m.4290T>C	rs121434469
NC_012920.1(MT-TI):m.4320C>A	rs1603219406
NC_012920.1(MT-TI):m.4320C>T	rs1603219406
NC_012920.1(MT-TI):m.4327T>C	rs1603219411

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