Variants studied for Hypertrophic cardiomyopathy 12

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
4	5	38	3	3	1	51

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
CSRP3	4	5	38	3	3	1	51

Submitter and significance breakdown #

Total submitters: 15

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Illumina Laboratory Services, Illumina	0	0	25	3	3	0	31
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	2	4	0	0	0	6
OMIM	4	0	0	0	0	0	4
Agnes Ginges Centre for Molecular Cardiology, Centenary Institute	0	0	2	0	0	0	2
Laboratory of Genetics and Molecular Cardiology, University of São Paulo	0	1	1	0	0	0	2
Genetics and Molecular Pathology, SA Pathology	0	0	2	0	0	0	2
Baylor Genetics	0	0	1	0	0	0	1
ClinVar Staff, National Center for Biotechnology Information (NCBI)	0	0	0	0	0	1	1
Petrovsky National Research Centre of Surgery, The Federal Agency for Scientific Organizations	0	0	1	0	0	0	1
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare	0	1	0	0	0	0	1
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	0	1	0	0	0	1
3billion	0	0	1	0	0	0	1
Institute of Immunology and Genetics Kaiserslautern	0	1	0	0	0	0	1
KardioGenetik, Herz- und Diabeteszentrum NRW	0	1	0	0	0	0	1
Regional Center For Medical Genetics Timis, Louis Turcanu Emergency Hospital for Children Timisoara	0	0	1	0	0	0	1

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