Variants studied for Microcephaly 16, 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
6	0	8	0	10	23

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	uncertain significance	benign	total
ANKLE2	6	8	10	23

Submitter and significance breakdown #

Total submitters: 9

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Submitter	pathogenic	uncertain significance	benign	total
Genome-Nilou Lab	0	0	10	10
OMIM	6	0	0	6
Baylor Genetics	0	2	0	2
Mendelics	0	1	0	1
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	1	0	1
Department of Medical Genetics, Sanjay Gandhi Post Graduate Institute of Medical Sciences	0	1	0	1
Geisinger Autism and Developmental Medicine Institute, Geisinger Health System	0	1	0	1
Johns Hopkins Genomics, Johns Hopkins University	0	1	0	1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	0	1	0	1

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