ClinVar Miner

Variants studied for Familial meningioma

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 risk factor total
29 17 473 264 18 5 804

Gene and significance breakdown #

Total genes and gene combinations: 8
Download table as spreadsheet
Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign risk factor total
SMARCE1 24 12 384 264 13 4 699
NF2 1 1 42 0 0 0 44
SUFU 0 1 35 0 5 1 42
LOC130004614, SUFU 0 0 8 0 0 0 8
PTEN 4 2 2 0 0 0 8
IQCJ-SCHIP1, SCHIP1 0 1 0 0 0 0 1
MN1 0 0 1 0 0 0 1
PDGFB 0 0 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 11
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign benign risk factor total
Invitae 22 8 379 264 13 0 686
Baylor Genetics 1 2 111 0 0 0 114
Centre for Mendelian Genomics, University Medical Centre Ljubljana 4 2 7 0 0 0 13
OMIM 0 0 0 0 0 5 5
KCCC/NGS Laboratory, Kuwait Cancer Control Center 0 0 0 0 5 0 5
Genetics and Molecular Pathology, SA Pathology 1 2 0 0 0 0 3
Genetic Services Laboratory, University of Chicago 1 1 0 0 0 0 2
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 0 1 0 0 0 1
Medical Genetics, Meyer Children Hospital 1 0 0 0 0 0 1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 0 1 0 0 0 0 1
Genomics England Pilot Project, Genomics England 0 1 0 0 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.