Variants studied for Hydrocephalus, nonsyndromic, autosomal recessive 1

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
7	2	14	3	9	35

Gene and significance breakdown #

Total genes and gene combinations: 3

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
CCDC88C	6	2	14	3	8	33
CCDC88C, LOC130056326	0	0	0	0	1	1
FSD1L	1	0	0	0	0	1

Submitter and significance breakdown #

Total submitters: 13

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Genome-Nilou Lab	0	0	0	0	9	9
OMIM	4	0	0	0	0	4
Baylor Genetics	0	0	4	0	0	4
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	0	1	3	0	0	4
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	0	2	0	0	2
Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics	1	0	1	0	0	2
New York Genome Center	0	0	2	0	0	2
3billion, Medical Genetics	0	0	0	2	0	2
Neuberg Centre For Genomic Medicine, NCGM	0	1	1	0	0	2
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	1	0	0	0	0	1
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	0	1	0	0	1
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	0	0	0	1	0	1
Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine	1	0	0	0	0	1

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