Variants studied for amelogenesis imperfecta type 1G

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
16	8	14	12	3	53

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
FAM20A, PRKAR1A	9	6	8	5	2	30
FAM20A	7	2	6	7	1	23

Submitter and significance breakdown #

Total submitters: 15

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Fulgent Genetics, Fulgent Genetics	3	0	10	12	1	26
OMIM	9	0	0	0	0	9
Reference Center For Rare Oral And Dental Diseases, Crmr O-rares, Hôpitaux Universitaires De Strasbourg	0	3	3	0	0	6
Center of Excellence in Genomics and Precision Dentistry, Faculty of Dentistry, Chulalongkorn University	2	2	0	0	0	4
Revvity Omics, Revvity	1	0	1	0	0	2
Genome-Nilou Lab	0	0	0	0	2	2
Baylor Genetics	1	0	0	0	0	1
Institute of Human Genetics, University of Ulm	1	0	0	0	0	1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	1	0	0	0	0	1
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	1	0	0	0	1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology	1	0	0	0	0	1
Medical Molecular Genetics, National Research Centre	0	1	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	1	0	0	0	1
Wang Lab, School of Dentistry, National Taiwan University	1	0	0	0	0	1
Clinical Laboratory Sciences Program (CLSP), King Saud bin Abdulaziz University for Health Sciences (KSAU-HS)	1	0	0	0	0	1

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