ClinVar Miner

List of variants in gene MT-TF reported as uncertain significance for Mitochondrial disease

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-CYB):m.583G>A	rs118203885
NC_012920.1(MT-CYB):m.590A>G	rs2068676854
NC_012920.1(MT-TF):m.622G>A	rs118203887

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