Variants studied for Microcephaly 9, primary, autosomal recessive

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
15	11	108	12	16	153

Gene and significance breakdown #

Total genes and gene combinations: 1

Download table as spreadsheet

Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
CEP152	15	11	108	12	16	153

Submitter and significance breakdown #

Total submitters: 16

Download table as spreadsheet

Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	0	72	12	16	100
Genetic Services Laboratory, University of Chicago	6	1	34	0	0	41
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	3	1	1	0	0	5
Baylor Genetics	0	0	4	0	0	4
OMIM	3	0	0	0	0	3
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	1	2	0	0	3
Service de Génétique Moléculaire, Hôpital Robert Debré	2	1	0	0	0	3
Institut de Recherche Interdisciplinaire en Biologie Humaine et Moleculaire, Universite Libre de Bruxelles	0	3	0	0	0	3
MGZ Medical Genetics Center	2	0	0	0	0	2
3billion	2	0	0	0	0	2
Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet	0	1	0	0	0	1
Courtagen Diagnostics Laboratory, Courtagen Life Sciences	1	0	0	0	0	1
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City	0	1	0	0	0	1
Molecular Diagnostics Laboratory, M Health Fairview: University of Minnesota	0	1	0	0	0	1
Genome-Nilou Lab	0	0	0	0	1	1
Human Genetics Bochum, Ruhr University Bochum	0	1	0	0	0	1

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.