ClinVar Miner

Variants studied for angioedema, hereditary, type 1/2

Included ClinVar conditions (3):
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
44 5 3 0 2 54

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign total
SERPING1 44 5 3 2 54

Submitter and significance breakdown #

Total submitters: 10
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Submitter pathogenic likely pathogenic uncertain significance benign total
Department of Immunology and Histocompatibility, University of Thessaly 26 3 1 0 30
OMIM 16 0 0 0 16
Central Haematology Laboratory,Luzerner Kantonsspital 2 0 1 0 3
Genome Diagnostics Laboratory,University Medical Center Utrecht 0 0 0 2 2
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen 0 0 0 2 2
Division of Rheumatology, Allergy and Immunology, UCSD 0 1 0 0 1
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 1 0 1
HSP Biomedical Diagnostics Department,Hospital San Pedro 1 0 0 0 1
ATS GeneTech Pvt Ltd 0 1 0 0 1
Diagnostics Lab (ASPIRE), CSIR - Centre for Cellular and Molecular Biology 1 0 0 0 1

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