ClinVar Miner

Variants studied for Leber congenital amaurosis 13

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
96 69 148 243 8 3 528

Gene and significance breakdown #

Total genes and gene combinations: 5
Download table as spreadsheet
Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
GPHN, RDH12 63 45 95 163 5 2 349
GPHN, RDH12, ZFYVE26 33 22 48 80 3 1 172
RDH12 0 2 3 0 0 0 5
ARG2, ATP6V1D, EIF2S1, FUT8, GARIN2, GPHN, PALS1, PIGH, PLEK2, PLEKHH1, RAD51B, RDH11, RDH12, TMEM229B, VTI1B, ZFYVE26 0 0 1 0 0 0 1
RDH11, RDH12, ZFYVE26 0 0 1 0 0 0 1

Submitter and significance breakdown #

Total submitters: 30
Download table as spreadsheet
Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Labcorp Genetics (formerly Invitae), Labcorp 84 19 141 243 6 0 493
Baylor Genetics 39 31 0 0 0 0 70
Laboratory of Genetics in Ophthalmology, Institut Imagine 21 6 0 0 0 0 27
OMIM 14 0 0 0 0 0 14
Ocular Genomics Institute, Massachusetts Eye and Ear 4 6 2 0 0 0 12
Mendelics 5 5 0 0 0 0 10
Fulgent Genetics, Fulgent Genetics 4 2 4 0 0 0 10
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard 1 3 2 0 0 0 6
Genome-Nilou Lab 1 0 2 0 3 0 6
3billion 1 3 2 0 0 0 6
Revvity Omics, Revvity 2 2 0 0 0 0 4
MGZ Medical Genetics Center 1 1 1 0 0 0 3
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center 2 0 1 0 0 0 3
Centre for Mendelian Genomics, University Medical Centre Ljubljana 2 1 0 0 0 0 3
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen 2 0 0 0 0 0 2
GenomeConnect - Invitae Patient Insights Network 0 0 0 0 0 2 2
DBGen Ocular Genomics 1 0 1 0 0 0 2
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 0 0 0 1 0 1
GeneReviews 0 0 0 0 0 1 1
Division of Human Genetics, Children's Hospital of Philadelphia 0 1 0 0 0 0 1
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare 0 1 0 0 0 0 1
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota 0 1 0 0 0 0 1
Breda Genetics srl 1 0 0 0 0 0 1
DASA 1 0 0 0 0 0 1
Neuberg Centre For Genomic Medicine, NCGM 1 0 0 0 0 0 1
Division of Molecular and Cellular Biology, National Hospital Organization Tokyo Medical Center 0 0 1 0 0 0 1
Pangenia Genomics, Pangenia Inc. 0 0 1 0 0 0 1
Payam Genetics Center, General Welfare Department of North Khorasan Province 1 0 0 0 0 0 1
Department of Medical Genetics, Erciyes University Faculty of Medicine 0 1 0 0 0 0 1
Dr.Nikuei Genetic Center 1 0 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.