ClinVar Miner

Variants studied for apparent mineralocorticoid excess

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 total
13 2 7 0 1 21

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance benign total
HSD11B2 13 2 7 1 21

Submitter and significance breakdown #

Total submitters: 8
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Submitter pathogenic likely pathogenic uncertain significance benign total
OMIM 11 0 0 0 11
Department of Genetics,Sultan Qaboos University Hospital, Oman 0 0 4 0 4
Biochemical Molecular Genetic Laboratory,King Abdulaziz Medical City 0 1 1 0 2
Molecular Biology Laboratory, Fundació Puigvert 1 1 0 0 2
Baylor Genetics 0 0 1 0 1
Integrated Genetics/Laboratory Corporation of America 0 0 0 1 1
Institute of Human Genetics, Klinikum rechts der Isar 1 0 0 0 1
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare 0 0 1 0 1

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