Variants studied for Congenital heart defects, multiple types, 4

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
13	5	22	25	4	69

Gene and significance breakdown #

Total genes and gene combinations: 3

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
NR2F2	10	5	22	25	4	66
CRELD1	2	0	0	0	0	2
BMP7	1	0	0	0	0	1

Submitter and significance breakdown #

Total submitters: 14

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Invitae	2	0	17	25	4	48
OMIM	7	0	0	0	0	7
Cytogenetics- Mohapatra Lab, Banaras Hindu University	3	0	0	0	0	3
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	1	1	0	0	2
Baylor Genetics	0	0	1	0	0	1
Mayo Clinic Laboratories, Mayo Clinic	0	1	0	0	0	1
Illumina Laboratory Services, Illumina	1	0	0	0	0	1
Molecular Genetics Department, Kulakov National Medical Research Center for Obstetrics, Gynecology and Perinatology	0	1	0	0	0	1
Cardiovascular Research Laboratory, Shanghai Chest Hospital, Shanghai Jiao Tong University	1	0	0	0	0	1
Institute of Human Genetics, University Hospital of Duesseldorf	0	1	0	0	0	1
Undiagnosed Diseases Network, NIH	0	0	1	0	0	1
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City	0	0	1	0	0	1
Medical Genetics Lab, Policlinico S. Orsola.Malpighi	0	1	0	0	0	1
3billion	0	0	1	0	0	1

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