List of variants in gene MT-TL2 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-TL2):m.12278T>C	rs1603223646
NC_012920.1(MT-TL2):m.12291T>C	rs1603223653
NC_012920.1(MT-TL2):m.12293G>A	rs1603223654
NC_012920.1(MT-TL2):m.12302C>A	rs1603223658
NC_012920.1(MT-TL2):m.12302C>T	rs1603223658
NC_012920.1(MT-TL2):m.12318G>A	rs1603223664

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