Variants studied for Familial partial lipodystrophy, Dunnigan type

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
17	10	32	6	14	77

Gene and significance breakdown #

Total genes and gene combinations: 3

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
LMNA	16	9	31	5	12	71
LMNA, LOC126805877	1	0	1	1	1	4
LMNA, LOC129931597	0	1	0	0	1	2

Submitter and significance breakdown #

Total submitters: 17

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	0	20	6	14	40
OMIM	12	0	0	0	0	12
Genetic Services Laboratory, University of Chicago	7	2	0	0	0	9
Institute of Human Genetics, University of Leipzig Medical Center	1	5	0	0	0	6
New York Genome Center	0	0	6	0	0	6
3billion	0	0	3	0	0	3
Neuberg Centre For Genomic Medicine, NCGM	2	1	0	0	0	3
Women's Health and Genetics/Laboratory Corporation of America, LabCorp	2	0	0	0	0	2
CSER _CC_NCGL, University of Washington	1	0	1	0	0	2
Baylor Genetics	0	1	0	0	0	1
Athena Diagnostics	1	0	0	0	0	1
Greenwood Genetic Center Diagnostic Laboratories, Greenwood Genetic Center	1	0	0	0	0	1
Mendelics	1	0	0	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	1	0	0	0	0	1
Clinical Genomics Laboratory, Washington University in St. Louis	0	0	1	0	0	1
Institute of Human Genetics, University Hospital Muenster	0	1	0	0	0	1
Molecular Genetics, Royal Melbourne Hospital	0	0	1	0	0	1

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