Variants studied for Factor XIII, b subunit, deficiency of

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
6	1	48	2	4	61

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	total
F13B	6	1	48	2	4	61

Submitter and significance breakdown #

Total submitters: 10

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	0	38	2	4	44
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	1	0	6	0	0	7
OMIM	4	0	0	0	0	4
Genome-Nilou Lab	0	0	0	0	3	3
Zotz-Klimas Genetics Lab, MVZ Zotz Klimas	0	0	2	0	0	2
Baylor Genetics	0	0	1	0	0	1
Revvity Omics, Revvity	0	1	0	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	1	0	0	0	0	1
Fulgent Genetics, Fulgent Genetics	0	0	1	0	0	1
ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology	0	0	1	0	0	1

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