Variants studied for Fliedner-Zweier syndrome

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)

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	9	3	0	0	21

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	total
SCAF4	10	8	3	20
LOC130066536, SCAF4	0	1	0	1

Submitter and significance breakdown #

Total submitters: 13

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Submitter	pathogenic	likely pathogenic	uncertain significance	total
Institute of Human Genetics, University of Leipzig Medical Center	2	1	1	4
OMIM	4	0	0	4
Juno Genomics, Hangzhou Juno Genomics, Inc	0	1	1	2
Molecular Genetics Laboratory, Motol Hospital	1	1	0	2
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	2	0	0	2
3billion	0	1	0	1
Clinical Genetics Laboratory, University Hospital Schleswig-Holstein	0	0	1	1
Clinical Genomics Laboratory, Washington University in St. Louis	1	0	0	1
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology	0	1	0	1
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center	0	1	0	1
Institute of Immunology and Genetics Kaiserslautern	0	1	0	1
Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen	0	1	0	1
Pediatric/Medical Genetics, Ministry of Health, Qatif Central Hospital	0	1	0	1

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