ClinVar Miner

Variants studied for gingival disorder

Included ClinVar conditions (8):
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
22 9 336 156 81 591

Gene and significance breakdown #

Total genes and gene combinations: 7
Download table as spreadsheet
Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
SOS1 13 4 216 79 61 363
FPR1 0 0 113 70 18 201
LOC129933535, SOS1 0 0 6 5 2 13
REST 6 4 1 2 0 10
KCNK4, KCNK4-CATSPERZ 2 0 0 0 0 2
​intergenic 0 1 0 0 0 1
RET 1 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 18
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Genome-Nilou Lab 0 1 113 68 24 206
Labcorp Genetics (formerly Invitae), Labcorp 0 0 113 70 18 201
Illumina Laboratory Services, Illumina 0 0 81 7 44 132
Fulgent Genetics, Fulgent Genetics 7 1 65 16 2 91
Centre for Mendelian Genomics, University Medical Centre Ljubljana 1 1 7 0 0 9
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 3 1 2 1 0 7
OMIM 4 0 0 0 0 4
Baylor Genetics 2 0 1 0 0 3
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine 0 3 0 0 0 3
Tartaglia Lab, Genetics and Rare Diseases Research Division, Bambino Gesu' Children's Hospital 2 0 0 0 0 2
Wang Lab, School of Dentistry, National Taiwan University 2 0 0 0 0 2
Mendelics 1 0 0 0 0 1
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München 0 1 0 0 0 1
Talkowski Laboratory, Center for Human Genetic Research, Massachusetts General Hospital 0 1 0 0 0 1
Institute of Human Genetics, Heidelberg University 1 0 0 0 0 1
Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine 1 0 0 0 0 1
Clinical Genomics Laboratory, Stanford Medicine 0 0 1 0 0 1
3billion 0 0 0 1 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.