ClinVar Miner

Variants studied for ACTH-independent macronodular adrenal hyperplasia 2

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:

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
16 8 13 3 0 39

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 total
ARMC5 13 8 13 2 35
ARMC5, LOC130058906 3 0 0 1 4

Submitter and significance breakdown #

Total submitters: 17
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Submitter pathogenic likely pathogenic uncertain significance likely benign total
OMIM 8 0 0 0 8
Fulgent Genetics, Fulgent Genetics 0 2 2 2 6
Molecular Medicine Laboratory, University of Brescia 3 3 0 0 6
Department of Pathology and Laboratory Medicine, Sinai Health System 0 0 2 1 3
3billion 0 0 2 0 2
Baylor Genetics 0 0 2 0 2
Genetics and Molecular Pathology, SA Pathology 2 0 0 0 2
Revvity Omics, Revvity 1 0 1 0 2
Clinical Genetics and Genomics, Karolinska University Hospital 1 0 0 0 1
Clinical Genomics, G42 Labs 0 1 0 0 1
Department of Human Genetics, Hannover Medical School 0 0 1 0 1
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre 0 0 1 0 1
Institute for Genomic Medicine (IGM) Clinical Laboratory, Nationwide Children's Hospital 0 0 1 0 1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein 0 0 1 0 1
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine 0 1 0 0 1
Payam Genetics Center, General Welfare Department of North Khorasan Province 1 0 0 0 1
Translational Medicine Institute, Shanxi Medical University 0 1 0 0 1

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