Variants in gene MID2 - 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
0	0	26	1	2	29

Condition and significance breakdown #

Total conditions: 3

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Condition	uncertain significance	likely benign	benign	total
not specified	19	0	0	19
not provided	5	1	2	8
Intellectual disability, X-linked 101	4	0	1	5

Submitter and significance breakdown #

Total submitters: 14

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Submitter	uncertain significance	likely benign	benign	total
Ambry Genetics	15	0	0	15
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	3	0	0	3
CeGaT Center for Human Genetics Tuebingen	3	0	0	3
Labcorp Genetics (formerly Invitae), Labcorp	1	0	1	2
Baylor Genetics	1	0	0	1
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center	1	0	0	1
Genetic Services Laboratory, University of Chicago	1	0	0	1
Genomic Research Center, Shahid Beheshti University of Medical Sciences	1	0	0	1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology	1	0	0	1
Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics	0	1	0	1
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital	1	0	0	1
Clinical Genetics Laboratory, Skane University Hospital Lund	1	0	0	1
Genome-Nilou Lab	0	0	1	1
Breakthrough Genomics, Breakthrough Genomics	0	0	1	1

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