ClinVar Miner

Variants studied for brittle cornea syndrome 1

Included ClinVar conditions (1):
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
6 3 222 58 31 2 320

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
ZNF469 6 3 199 55 28 2 291
PRDM5 0 0 23 3 3 0 29

Submitter and significance breakdown #

Total submitters: 15
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Illumina Clinical Services Laboratory,Illumina 0 0 198 54 29 0 281
Genome Diagnostics Laboratory,VU University Medical Center Amsterdam 0 0 0 2 18 0 20
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 0 0 0 18 0 18
Baylor Genetics 0 0 13 0 0 0 13
Fulgent Genetics,Fulgent Genetics 0 0 11 0 0 0 11
Center for Medical Genetics Ghent,University of Ghent 2 3 0 0 0 0 5
OMIM 4 0 0 0 0 0 4
Centre for Mendelian Genomics,University Medical Centre Ljubljana 0 0 3 0 0 0 3
Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago 0 0 1 2 0 0 3
Mendelics 0 0 0 0 2 0 2
GenomeConnect, ClinGen 0 0 0 0 0 2 2
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center 0 0 0 1 1 0 2
Institute of Human Genetics,Cologne University 0 0 1 0 0 0 1
Knight Diagnostic Laboratories, Oregon Health and Sciences University 0 0 1 0 0 0 1
Nilou-Genome Lab 0 0 0 0 1 0 1

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