ClinVar Miner

Variants studied for adrenal gland pheochromocytoma

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
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Gene type:
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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
32 31 248 60 114 478

Gene and significance breakdown #

Total genes and gene combinations: 14
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
RET 8 0 77 24 47 155
TMEM127 4 20 74 13 28 133
MAX 0 0 30 8 24 62
KIF1B 1 0 20 4 2 27
SDHC 0 0 21 2 2 25
SDHD 6 2 5 6 5 24
SDHB 8 4 8 0 1 21
LOC106736614, RET 0 0 5 1 2 8
LOC107303340, VHL 2 4 0 0 0 6
SDHAF2 0 0 6 0 0 6
SDHA 0 0 2 2 0 4
VHL 3 1 0 0 0 4
MPZ, SDHC 0 0 0 0 2 2
CFAP126, SDHC 0 0 0 0 1 1

Submitter and significance breakdown #

Total submitters: 17
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Illumina Clinical Services Laboratory,Illumina 0 0 232 55 113 400
OMIM 26 0 0 0 0 26
Familial Cancer Clinic,Veneto Institute of Oncology 0 19 0 0 0 19
Endocrinology Clinic, Seth G.S. Medical College 0 10 0 0 0 10
Baylor Genetics 1 1 6 0 0 8
CSER _CC_NCGL, University of Washington 0 0 4 3 0 7
Mendelics 1 0 1 1 0 3
Fulgent Genetics,Fulgent Genetics 0 0 3 0 0 3
Centre for Mendelian Genomics,University Medical Centre Ljubljana 0 0 2 0 0 2
Genetic Services Laboratory, University of Chicago 1 0 0 0 0 1
Institute of Human Genetics,Cologne University 0 0 1 0 0 1
Integrated Genetics/Laboratory Corporation of America 0 0 0 0 1 1
Center of Genomic medicine, Geneva,University Hospital of Geneva 1 0 0 0 0 1
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 0 0 1 0 1
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota 1 0 0 0 0 1
Division of Medical Genetics, University of Washington 1 0 0 0 0 1
New York Genome Center 0 1 0 0 0 1

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