Variants studied for Tooth agenesis, selective, 7

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
15	4	1	0	0	20

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	total
LRP6	15	4	1	20

Submitter and significance breakdown #

Total submitters: 12

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Submitter	pathogenic	likely pathogenic	uncertain significance	total
OMIM	4	0	0	4
Revvity Omics, Revvity	0	2	1	3
Department of Prosthodontics, Peking University School and Hospital of Stomatology	3	0	0	3
Center of Excellence in Genomics and Precision Dentistry, Faculty of Dentistry, Chulalongkorn University	1	1	0	2
Baylor Genetics	1	0	0	1
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center	1	0	0	1
Department of Clinical Genetics, Copenhagen University Hospital, Rigshospitalet	1	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	1	0	0	1
Illumina Laboratory Services, Illumina	1	0	0	1
Undiagnosed Diseases Network, NIH	1	0	0	1
Research Center of Stomatology, College of Stomatology, Xi'an Jiaotong University	0	1	0	1
State Key Laboratory of Oral & Maxillofacial Reconstruction and Regeneration, Key Laboratory of Oral Biomedicine Ministry of Education, Hubei Key Laboratory of Stomatology, School & Hospital of Stomatology, Wuhan University	1	0	0	1

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