ClinVar Miner

Variants studied for Immunodeficiency 11; B-cell expansion with NFKB and T-cell anergy; IMMUNODEFICIENCY 11B WITH ATOPIC DERMATITIS

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
0 0 4 0 0 4

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination uncertain significance total
CARD11 4 4

Submitter and significance breakdown #

Total submitters: 3
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Submitter uncertain significance total
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 2 2
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic 1 1
Fulgent Genetics,Fulgent Genetics 1 1

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