Variants studied for apparent mineralocorticoid excess

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		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	10	62	4	3	89

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	10	62	4	3	89

Submitter and significance breakdown #

Total submitters: 16

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Fulgent Genetics, Fulgent Genetics	1	8	52	4	0	65
OMIM	11	0	0	0	0	11
Department Of Genetics, Sultan Qaboos University Hospital, Sultan Qaboos University	1	0	3	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
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	0	0	1	0	0	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
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital	0	1	0	0	0	1
Pediatrics Genetics, Post Graduate Institute of Medical Education and Research	0	0	1	0	0	1
3billion, Medical Genetics	0	1	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	0	1	0	0	1

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