ClinVar Miner

Variants studied for 46,XX disorder of sex development induced by fetal androgens excess

Included ClinVar conditions (6):
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 not provided total
89 37 76 20 6 7 226

Gene and significance breakdown #

Total genes and gene combinations: 9
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign not provided total
NR3C1 8 0 47 20 0 0 75
CYP11B1, LOC106799833 12 19 18 0 0 6 49
CYP21A2, LOC106780800 22 5 1 0 5 1 33
CYP21A2 20 1 1 0 0 0 22
CYP11B1 10 6 5 0 0 0 20
POR 7 3 4 0 0 0 13
HSD3B2 10 1 0 0 0 0 11
CYP11B1, LOC110673972 0 2 0 0 0 0 2
CYP21A2, LOC106780800, TNXB 0 0 0 0 1 0 1

Submitter and significance breakdown #

Total submitters: 20
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign not provided total
Illumina Clinical Services Laboratory,Illumina 0 1 51 20 0 0 72
Counsyl 22 28 20 0 0 0 70
OMIM 66 0 0 0 0 0 66
GeneReviews 12 0 0 0 5 0 17
Fulgent Genetics 7 1 1 0 0 0 9
Invitae 2 1 3 0 0 0 6
Pediatric Endocrinology Laboratory; Christian Albrechts University of Kiel 0 0 0 0 0 6 6
GenePathDx,Causeway Health Care Private Ltd 0 4 0 0 0 0 4
Soonchunhyang University Bucheon Hospital,Soonchunhyang University Medical Center 0 2 1 0 0 0 3
Athena Diagnostics Inc 0 0 0 0 2 0 2
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine 1 1 0 0 0 0 2
Institute of Human Genetics,Klinikum rechts der Isar 2 0 0 0 0 0 2
Genomic Research Center,Shahid Beheshti University of Medical Sciences 2 0 0 0 0 0 2
Shenzhen Institute of Pediatrics,Shenzhen Children's Hospital 2 0 0 0 0 0 2
Knight Diagnostic Laboratories,Oregon Health and Sciences University 2 0 0 0 0 0 2
Bioscientia Institut fuer Medizinische Diagnostik GmbH,Sonic Healthcare 0 0 2 0 0 0 2
Foundation for Research in Genetics and Endocrinology,Institute of Human Genetics 1 0 0 0 0 0 1
Equipe Genetique des Anomalies du Developpement,Université de Bourgogne 1 0 0 0 0 0 1
Centro de Desenvolvimento Científico e Tecnológico,Secretaria da Saúde do Estado do Rio Grande do Sul 0 0 0 0 0 1 1
Biochemical Molecular Genetic Laboratory,King Abdulaziz Medical City 1 0 0 0 0 0 1

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