Variants in gene ALG11 - 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	total
6	2	41	22	5	72

Condition and significance breakdown #

Total conditions: 5

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Condition	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
ALG11-congenital disorder of glycosylation	6	0	28	9	3	46
not provided	0	2	11	10	2	25
Inborn genetic diseases	0	0	8	0	0	8
ALG11-related condition	0	0	0	3	1	4
not specified	0	0	0	2	2	4

Submitter and significance breakdown #

Total submitters: 15

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Invitae	0	0	18	14	3	35
GeneDx	0	2	6	5	4	17
Illumina Laboratory Services, Illumina	0	0	10	0	2	12
Ambry Genetics	0	0	8	0	0	8
OMIM	6	0	0	0	0	6
Eurofins Ntd Llc (ga)	0	0	4	0	1	5
PreventionGenetics, part of Exact Sciences	0	0	0	3	1	4
Revvity Omics, Revvity	0	0	2	0	0	2
CeGaT Center for Human Genetics Tuebingen	0	0	1	1	0	2
Baylor Genetics	0	0	1	0	0	1
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia	0	0	0	0	1	1
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics	0	0	0	1	0	1
New York Genome Center	0	0	1	0	0	1
3billion	0	0	1	0	0	1
Neuberg Supratech Reference Laboratories Pvt Ltd, Neuberg Centre for Genomic Medicine	0	0	1	0	0	1

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