List of variants in gene MT-TK reported as likely pathogenic 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-TK):m.8313G>A	rs118192101
NC_012920.1(MT-TK):m.8340G>A	rs2521961657
NC_012920.1(MT-TK):m.8356T>C	rs118192099
NC_012920.1(MT-TK):m.8363G>A	rs118192100

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