ClinVar Miner

List of variants in gene MT-TR reported as uncertain significance for MELAS syndrome

Included ClinVar conditions (6):

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: 3

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TR):m.10405T>C	rs1603222825
NC_012920.1(MT-TR):m.10457T>C	rs1603222845
NC_012920.1(MT-TR):m.10462T>C	rs1603222850

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