ClinVar Miner

Variants studied for factor XIII deficiency

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
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
33 14 113 9 21 186

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
F13A1 27 13 65 7 17 125
F13B 6 1 48 2 4 61

Submitter and significance breakdown #

Total submitters: 23
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services, Illumina 1 0 91 9 16 117
OMIM 23 0 0 0 0 23
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 2 2 12 0 0 16
Genome-Nilou Lab 0 0 0 0 11 11
ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology 0 3 3 0 0 6
Zotz-Klimas Genetics Lab, MVZ Zotz Klimas 0 1 4 0 0 5
NIHR Bioresource Rare Diseases, University of Cambridge 0 4 0 0 0 4
Revvity Omics, Revvity 1 2 0 0 0 3
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 3 0 0 0 0 3
Fulgent Genetics, Fulgent Genetics 0 0 2 0 0 2
3billion 1 0 1 0 0 2
Baylor Genetics 0 0 1 0 0 1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute 1 0 0 0 0 1
Knight Diagnostic Laboratories, Oregon Health and Sciences University 0 0 1 0 0 1
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues 1 0 0 0 0 1
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 0 1 0 0 0 1
Medical Genetics, Necip Fazıl Sehir Hastanesi 1 0 0 0 0 1
Hematology and Blood Transfusion, Iran University of Medical Sciences 1 0 0 0 0 1
Human Genetics Section, Sidra Medicine 0 1 0 0 0 1
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology 0 1 0 0 0 1
Institute of Human Genetics, University Hospital Muenster 1 0 0 0 0 1
Suma Genomics, Suma Genomics 0 0 1 0 0 1
Neuberg Centre For Genomic Medicine, NCGM 0 0 1 0 0 1

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