Variants in gene HOMER2 - ClinVar Miner

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	total
3	2	83	74	43	184

Condition and significance breakdown #

Total conditions: 5

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Condition	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
not provided	0	0	53	64	43	144
Inborn genetic diseases	0	0	32	0	0	32
HOMER2-related disorder	0	0	5	9	4	18
not specified	0	0	1	7	8	16
Autosomal dominant nonsyndromic hearing loss 68	3	2	3	1	0	9

Submitter and significance breakdown #

Total submitters: 17

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Labcorp Genetics (formerly Invitae), Labcorp	0	0	45	44	23	112
GeneDx	0	0	0	18	29	47
Ambry Genetics	0	0	32	0	0	32
Breakthrough Genomics, Breakthrough Genomics	0	0	0	4	17	21
PreventionGenetics, part of Exact Sciences	0	0	5	9	4	18
CeGaT Center for Human Genetics Tuebingen	0	0	0	9	0	9
Athena Diagnostics	0	0	1	0	6	7
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	0	0	1	5	0	6
Eurofins Ntd Llc (ga)	0	0	4	1	1	6
Department of Pathology and Laboratory Medicine, Sinai Health System	0	0	3	1	0	4
OMIM	2	0	0	0	0	2
Baylor Genetics	0	0	1	0	0	1
Mayo Clinic Laboratories, Mayo Clinic	0	0	1	0	0	1
Clinical Genomics Laboratory, Washington University in St. Louis	0	0	1	0	0	1
Precision Medicine Center, Zhengzhou University	0	1	0	0	0	1
Genetics Department, Hospital Ramon y Cajal-IRYCIS	1	0	0	0	0	1
Institute of Rare Diseases, West China Hospital, Sichuan University	0	1	0	0	0	1

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