Variants studied for Autosomal dominant nonsyndromic hearing loss 11; Autosomal recessive nonsyndromic hearing loss 2; Usher syndrome type 1

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
61	70	73	5	4	1	211

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
MYO7A	61	70	73	5	4	1	211

Submitter and significance breakdown #

Total submitters: 5

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Fulgent Genetics, Fulgent Genetics	55	68	57	5	4	0	189
Department of Pathology and Laboratory Medicine, Sinai Health System	2	0	12	0	0	0	14
Juno Genomics, Hangzhou Juno Genomics, Inc	6	2	6	0	0	0	14
Genetics and Molecular Pathology, SA Pathology	1	0	0	0	0	0	1
GenomeConnect, ClinGen	0	0	0	0	0	1	1

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