ClinVar Miner

Variants studied for Immunodeficiency, common variable, 13

Coded as:
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
8 2 0 0 1 11

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic benign total
IKZF1 8 2 1 11

Submitter and significance breakdown #

Total submitters: 4
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Submitter pathogenic likely pathogenic benign total
OMIM 6 0 0 6
Immunogenetics Laboratory,Johns Hopkins All Children's Hospital 1 2 0 3
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 0 1 1
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego 1 0 0 1

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