ClinVar Miner

List of variants in gene MT-TI reported as pathogenic for MERRF syndrome

Included ClinVar conditions (3):

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-TI):m.4284G>A	rs121434468
NC_012920.1(MT-TI):m.4296G>A	rs1603219393
m.4300A>G	rs121434470

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