List of variants in gene COX6B1 reported as likely benign for Mitochondrial complex 4 deficiency, nuclear type 7

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
NM_001863.5(COX6B1):c.107-16A>G	rs187740487	0.00049
NM_001863.5(COX6B1):c.243G>A (p.Thr81=)	rs141958404	0.00039
NM_001863.5(COX6B1):c.-11-8G>A	rs200312775	0.00005

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