ClinVar Miner

Variants studied for Apparent mineralocorticoid excess

Coded as:
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
13 3 14 4 3 34

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
HSD11B2 13 3 14 4 3 34

Submitter and significance breakdown #

Total submitters: 13
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
OMIM 11 0 0 0 0 11
Fulgent Genetics, Fulgent Genetics 1 1 3 4 0 9
Department Of Genetics, Sultan Qaboos University Hospital, Sultan Qaboos University 0 0 4 0 0 4
Revvity Omics, Revvity 0 0 3 0 0 3
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City 0 1 1 0 0 2
Genome-Nilou Lab 0 0 0 0 2 2
Molecular Biology Laboratory, Fundació Puigvert 1 1 0 0 0 2
Baylor Genetics 0 0 1 0 0 1
Women's Health and Genetics/Laboratory Corporation of America, LabCorp 0 0 0 0 1 1
Institute Of Human Genetics Munich, Klinikum Rechts Der Isar, Tu München 1 0 0 0 0 1
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare 0 0 1 0 0 1
3billion 0 1 0 0 0 1
Neuberg Supratech Reference Laboratories Pvt Ltd, Neuberg Centre for Genomic Medicine 0 0 1 0 0 1

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