ClinVar Miner

Variants in gene LAMC3

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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
6 2 61 87 66 179

Condition and significance breakdown #

Total conditions: 4
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Condition pathogenic likely pathogenic uncertain significance likely benign benign total
not specified 0 0 22 73 34 107
not provided 1 2 38 17 23 79
Cortical malformations, occipital 4 0 9 2 13 28
Inborn genetic diseases 1 0 1 0 0 2

Submitter and significance breakdown #

Total submitters: 12
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
GeneDx 0 1 16 47 46 110
Genetic Services Laboratory, University of Chicago 0 0 23 40 4 67
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics 1 0 17 2 11 31
Diagnostic Laboratory, Department of Genetics,University Medical Center Groningen 0 0 0 2 13 15
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics 0 0 5 9 0 14
CeGaT Praxis fuer Humangenetik Tuebingen 0 1 4 1 0 6
Fulgent Genetics,Fulgent Genetics 0 0 5 0 0 5
OMIM 4 0 0 0 0 4
Baylor Miraca Genetics Laboratories, 0 0 2 0 0 2
Ambry Genetics 1 0 1 0 0 2
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic 0 0 1 0 0 1
Genomic Research Center,Shahid Beheshti University of Medical Sciences 0 0 1 0 0 1

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