Variants studied for Combined oxidative phosphorylation defect type 24; Hearing loss, autosomal recessive 94

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:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
0	0	0	1	0	1	2

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	likely benign	not provided	total
NARS2	1	1	2

Submitter and significance breakdown #

Total submitters: 2

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Submitter	likely benign	not provided	total
GenomeConnect, ClinGen	0	1	1
3billion	1	0	1

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