Variants studied for Adams-Oliver syndrome 6

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
10	6	6	0	0	22

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	total
DLL4	10	6	6	22

Submitter and significance breakdown #

Total submitters: 12

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Submitter	pathogenic	likely pathogenic	uncertain significance	total
Centre of Medical Genetics, University of Antwerp	3	1	3	7
OMIM	6	0	0	6
Centogene AG - the Rare Disease Company	0	1	0	1
Fulgent Genetics, Fulgent Genetics	0	0	1	1
HudsonAlpha Institute for Biotechnology, HudsonAlpha Institute for Biotechnology	1	0	0	1
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City	0	1	0	1
Johns Hopkins Genomics, Johns Hopkins University	0	0	1	1
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology	0	1	0	1
3billion	0	1	0	1
Center of Medical Genomics-TUH, Thammasat University	0	1	0	1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	0	0	1	1
MVZ Medizinische Genetik Mainz	0	1	0	1

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