Variants studied for microcephaly 20, 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
10	4	16	2	3	33

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
KIF14	10	4	16	2	3	33

Submitter and significance breakdown #

Total submitters: 14

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Baylor Genetics	0	1	7	0	0	8
OMIM	7	0	0	0	0	7
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	4	0	0	4
Genome-Nilou Lab	0	0	0	0	3	3
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	1	1	0	0	0	2
Fulgent Genetics, Fulgent Genetics	0	0	0	2	0	2
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	0	1	1	0	0	2
Illumina Laboratory Services, Illumina	0	0	2	0	0	2
Neuberg Centre For Genomic Medicine, NCGM	0	1	1	0	0	2
Institute of Human Genetics, University of Goettingen	0	1	0	0	0	1
Institute of Human Genetics, University of Leipzig Medical Center	1	0	0	0	0	1
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard	0	0	1	0	0	1
Breda Genetics srl	0	0	1	0	0	1
Dr.Nikuei Genetic Center	1	0	0	0	0	1

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