ClinVar Miner

Variants studied for Bronchiectasis with or without elevated sweat chloride 2

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
4 0 35 7 43 87

Gene and significance breakdown #

Total genes and gene combinations: 2
Download table as spreadsheet
Gene or gene combination pathogenic uncertain significance likely benign benign total
SCNN1A 4 34 7 39 82
LTBR, SCNN1A 0 1 0 4 5

Submitter and significance breakdown #

Total submitters: 9
Download table as spreadsheet
Submitter pathogenic uncertain significance likely benign benign total
Illumina Laboratory Services, Illumina 0 27 7 42 76
Johns Hopkins Genomics, Johns Hopkins University 0 4 0 0 4
OMIM 3 0 0 0 3
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 2 0 0 2
Genome-Nilou Lab 0 0 0 2 2
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 0 1 0 0 1
Genetics and Molecular Pathology, SA Pathology 0 1 0 0 1
DASA 1 0 0 0 1
Clinical Laboratory Sciences Program (CLSP), King Saud bin Abdulaziz University for Health Sciences (KSAU-HS) 0 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.