Variants in gene DOCK4 - ClinVar Miner

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	not provided	total
0	4	157	25	18	2	205

Condition and significance breakdown #

Total conditions: 8

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Condition	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
not specified	0	124	1	0	0	125
not provided	0	17	21	16	1	54
DOCK4-related disorder	0	7	3	1	0	11
Neurodevelopmental disorder	3	8	0	0	0	11
See cases	0	0	1	1	0	2
Autism	1	0	0	0	0	1
Autism spectrum disorder	0	1	0	0	0	1
Normal pregnancy	0	0	0	0	1	1

Submitter and significance breakdown #

Total submitters: 15

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Submitter	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Ambry Genetics	0	124	1	0	0	125
Labcorp Genetics (formerly Invitae), Labcorp	0	3	14	13	0	30
CeGaT Center for Human Genetics Tuebingen	0	6	10	2	0	18
PreventionGenetics, part of Exact Sciences	0	7	3	1	0	11
Institute of Human Genetics, University of Leipzig Medical Center	3	8	0	0	0	11
Breakthrough Genomics, Breakthrough Genomics	0	0	3	4	0	7
Quest Diagnostics Nichols Institute San Juan Capistrano	0	5	0	0	0	5
GeneDx	0	0	0	2	0	2
Bionano Laboratories	0	2	0	0	0	2
Revvity Omics, Revvity	0	1	0	0	0	1
Department of Psychiatry, Nagoya University	1	0	0	0	0	1
ISCA Site 6	0	0	1	0	0	1
Institute of Molecular and Cell Biology, University of Tartu	0	0	0	0	1	1
Genetics and Molecular Pathology, SA Pathology	0	1	0	0	0	1
GenomeConnect - Brain Gene Registry	0	0	0	0	1	1

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