ClinVar Miner

Variants studied for Agammaglobulinemia 2, autosomal recessive

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 not provided total
3 0 126 67 23 2 212

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic uncertain significance likely benign benign not provided total
IGLL1 3 125 67 23 2 211
C22orf15, CHCHD10, DERL3, DRICH1, IGLL1, MIF, MMP11, RGL4, SLC2A11, SMARCB1, VPREB3, ZNF70 0 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 12
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Submitter pathogenic uncertain significance likely benign benign not provided total
Invitae 0 121 65 23 0 209
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 1 1 10 0 12
OMIM 3 0 0 0 0 3
Fulgent Genetics, Fulgent Genetics 0 2 1 0 0 3
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 1 2 0 0 0 3
New York Genome Center 0 3 0 0 0 3
Revvity Omics, Revvity Omics 0 2 0 0 0 2
Baylor Genetics 0 1 0 0 0 1
Mayo Clinic Laboratories, Mayo Clinic 0 1 0 0 0 1
3billion 1 0 0 0 0 1
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 1 1
GenomeConnect - Brain Gene Registry 0 0 0 0 1 1

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