ClinVar Miner

Variants in gene HOXB13

Minimum submission review status: Collection method:
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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 association total
1 1 1107 96 7 1 1200

Condition and significance breakdown #

Total conditions: 7
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Condition pathogenic likely pathogenic uncertain significance likely benign benign association total
Prostate cancer, hereditary, 1 0 0 762 0 0 0 762
not provided 1 1 293 52 1 1 345
Hereditary cancer-predisposing syndrome 0 1 206 62 3 0 271
not specified 0 0 0 3 3 0 6
Prostate cancer, hereditary, 9 1 0 4 0 0 0 5
Carcinoma of pancreas 0 1 0 0 0 0 1
Prostate cancer susceptibility 1 0 0 0 0 0 1

Submitter and significance breakdown #

Total submitters: 11
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign association total
Laboratory of Virology, Microbiology, Quality and Medical Biotechnologies, Faculty of Sciences and Techniques - Mohammedia, Hassan II University of Casablanca 0 0 762 0 0 0 762
Invitae 0 0 288 50 0 1 339
Ambry Genetics 0 1 205 62 3 0 271
GeneDx 1 0 10 6 4 0 21
Fulgent Genetics,Fulgent Genetics 0 0 4 0 0 0 4
CeGaT Praxis fuer Humangenetik Tuebingen 0 1 3 0 0 0 4
OMIM 1 0 0 0 0 0 1
Illumina Clinical Services Laboratory,Illumina 1 0 0 0 0 0 1
University of Washington Department of Laboratory Medicine, University of Washington 1 0 0 0 0 0 1
CZECANCA consortium 0 1 0 0 0 0 1
Department of Pediatric Oncology, Hematology and Clinical Immunology,University Clinics Duesseldorf 0 0 1 0 0 0 1

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