ClinVar Miner

List of variants in gene MT-CYB 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: 3

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.15150G>A	rs207460000
NC_012920.1(MT-CYB):m.15242G>A	rs207459999
m.14787_14790delTTAA	rs207460005

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