List of variants in gene MT-TG 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: 11

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TG):m.10005A>T	rs1603222621
NC_012920.1(MT-TG):m.10008A>G	rs1603222626
NC_012920.1(MT-TG):m.10014G>A	rs1603222629
NC_012920.1(MT-TG):m.10015T>C	rs28374827
NC_012920.1(MT-TG):m.10020T>C	rs1603222636
NC_012920.1(MT-TG):m.10027T>C	rs1603222638
NC_012920.1(MT-TG):m.10043del	rs1603222645
NC_012920.1(MT-TG):m.10048A>G	rs878957961
NC_012920.1(MT-TG):m.10055A>G	rs1603222653
NC_012920.1(MT-TG):m.9993T>C	rs1603222613
NC_012920.1(MT-TG):m.9996T>C	rs1556423755

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