ClinVar Miner

Variants studied for Multiple endocrine neoplasia type 2B

Coded as:
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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
8 16 48 34 25 123

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 total
RET 8 16 48 33 25 122
LOC110121502, MCS+9.7, RET 0 0 0 1 0 1

Submitter and significance breakdown #

Total submitters: 17
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Counsyl 1 1 40 25 4 71
KCCC/NGS Laboratory, Kuwait Cancer Control Center 2 0 2 12 21 37
Database of Curated Mutations (DoCM) 0 14 0 0 0 14
Centre for Mendelian Genomics, University Medical Centre Ljubljana 2 0 3 0 0 5
Genome-Nilou Lab 0 0 0 0 5 5
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne 0 0 3 0 1 4
Institute of Human Genetics, University of Leipzig Medical Center 1 0 1 2 0 4
OMIM 2 0 0 0 0 2
Laboratory of Molecular and Cytogenetics, Department of Anatomy, All India Institute of Medical Sciences (AIIMS) 1 1 0 0 0 2
Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital 1 0 0 0 0 1
MGZ Medical Genetics Center 1 0 0 0 0 1
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 1 0 0 0 0 1
Duke University Health System Sequencing Clinic, Duke University Health System 1 0 0 0 0 1
Myriad Genetics, Inc. 1 0 0 0 0 1
Division of Medical Genetics, Azienda Ospedaliero-Universitaria Policlinico S. Orsola-Malpighi 0 1 0 0 0 1
Suma Genomics 1 0 0 0 0 1
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein 1 0 0 0 0 1

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