ClinVar Miner

Variants studied for Agammaglobulinemia, non-Bruton type

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
23 0 2 0 0 2 26

Gene and significance breakdown #

Total genes and gene combinations: 4
Download table as spreadsheet
Gene or gene combination pathogenic uncertain significance not provided total
BTK 17 1 0 18
IGHM 5 0 0 5
IGH, IGHM 1 0 2 2
CD79A 0 1 0 1

Submitter and significance breakdown #

Total submitters: 5
Download table as spreadsheet
Submitter pathogenic uncertain significance not provided total
Clinical Molecular Genetics Laboratory,Johns Hopkins All Children's Hospital 17 1 0 18
OMIM 5 0 0 5
ClinVar Staff, National Center for Biotechnology Information (NCBI) 0 0 2 2
Genomic Research Center,Shahid Beheshti University of Medical Sciences 0 1 0 1
Fundacion Publica Galega de Medicina Xenomica,Servicio Galego de Saude 1 0 0 1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.