Variants studied for Stüve-Wiedemann syndrome 1

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
9	6	9	9	9	41

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
LIFR	9	6	9	9	9	41

Submitter and significance breakdown #

Total submitters: 13

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories	0	0	3	6	9	18
Fulgent Genetics, Fulgent Genetics	1	1	5	2	1	10
Revvity Omics, Revvity	3	2	1	0	0	6
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	1	0	0	1	0	2
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	0	1	0	0	0	1
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München	1	0	0	0	0	1
Department Of Genetics, Sultan Qaboos University Hospital, Sultan Qaboos University	1	0	0	0	0	1
Laboratory of Medical Genetics, National & Kapodistrian University of Athens	1	0	0	0	0	1
Division of Genetics, Dept of Pediatrics, All India Institute of Medical Sciences	0	1	0	0	0	1
3billion	1	0	0	0	0	1
Suma Genomics	1	0	0	0	0	1
Hacettepe Pediatric Genetics Laboratory, Hacettepe University	0	1	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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