Variants in gene HMMR - 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
0	2	61	5	5	72

Condition and significance breakdown #

Total conditions: 5

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Condition	likely pathogenic	uncertain significance	likely benign	benign	total
not specified	0	53	4	0	57
Familial cancer of breast	0	6	0	1	7
Ovarian cancer	2	0	0	2	4
not provided	0	1	1	2	4
Breast cancer, susceptibility to	0	1	0	0	1

Submitter and significance breakdown #

Total submitters: 9

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Submitter	likely pathogenic	uncertain significance	likely benign	benign	total
Ambry Genetics	0	53	4	0	57
Laboratory of Molecular Epidemiology of Birth Defects, West China Second University Hospital, Sichuan University	2	0	0	2	4
Department of Pathology and Laboratory Medicine, Sinai Health System	0	2	0	1	3
Labcorp Genetics (formerly Invitae), Labcorp	0	0	0	2	2
Neuberg Centre For Genomic Medicine, NCGM	0	2	0	0	2
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein	0	2	0	0	2
CeGaT Center for Human Genetics Tuebingen	0	0	1	0	1
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	1	0	0	1
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology	0	1	0	0	1

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