List of variants in gene MT-TL2 reported as uncertain significance by ClinGen Mitochondrial Disease Nuclear and Mitochondrial Variant Curation Expert Panel, ClinGen

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: 4

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TL2):m.12271T>C	rs1131692061
NC_012920.1(MT-TL2):m.12294G>A
NC_012920.1(MT-TL2):m.12316G>A
NC_012920.1(MT-TL2):m.12320A>G	rs121434463

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