Variants studied for Familial dysfibrinogenemia

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
16	14	10	0	0	38

Gene and significance breakdown #

Total genes and gene combinations: 3

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	total
FGG	8	8	2	16
FGA	7	4	1	12
FGB	1	2	7	10

Submitter and significance breakdown #

Total submitters: 14

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Submitter	pathogenic	likely pathogenic	uncertain significance	total
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	11	4	0	15
ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology	2	3	6	11
Genetics and Molecular Pathology, SA Pathology	2	2	1	5
Juno Genomics, Hangzhou Juno Genomics, Inc	2	1	1	4
Institute of Human Genetics, University Hospital Muenster	1	0	2	3
Zotz-Klimas Genetics Lab, MVZ Zotz Klimas	1	1	0	2
Baylor Genetics	1	0	0	1
Institute of Human Genetics, University of Goettingen	0	1	0	1
Laboratory of Medical Genetics, National & Kapodistrian University of Athens	1	0	0	1
Johns Hopkins Genomics, Johns Hopkins University	1	0	0	1
Biochemistry Laboratory, Bechir Hamza Children's Hospital	1	0	0	1
Lifecell International Pvt. Ltd	0	1	0	1
Institute of Immunology and Genetics Kaiserslautern	0	1	0	1
Molecular Genetics and NGS Laboratory, Hospital Fundacion Valle Del Lili	0	1	0	1

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