List of variants in gene MT-TL1 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: 8

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TL1):m.3243A>T	rs199474657
NC_012920.1(MT-TL1):m.3251A>G	rs199474662
NC_012920.1(MT-TL1):m.3255G>A	rs1603218856
NC_012920.1(MT-TL1):m.3256C>T	rs199474659
NC_012920.1(MT-TL1):m.3258T>C
NC_012920.1(MT-TL1):m.3260A>G	rs199474663
NC_012920.1(MT-TL1):m.3302A>G	rs1603218878
NC_012920.1(MT-TL1):m.3303C>T	rs199474660

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