ClinVar Miner

List of variants in gene MT-TW 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.5538G>A	rs1603220012
NC_012920.1(MT-CYB):m.5558A>G	rs370471013
NC_012920.1(MT-TW):m.5545C>T	rs387906418

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