Variants studied for Familial type 3 hyperlipoproteinemia

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	not provided	total
15	5	4	1	0	1	23

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	not provided	total
APOE	13	5	4	1	1	21
LDLR	2	0	0	0	0	2

Submitter and significance breakdown #

Total submitters: 10

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	not provided	total
OMIM	13	0	0	0	1	14
New York Genome Center	0	2	1	0	0	3
Cardiogenetic Research Center, Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences	2	0	0	0	0	2
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	0	1	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	0	1	0	0	1
Laboratory of Inherited Metabolic Diseases, Research centre for medical genetics	0	1	0	0	0	1
Reproductive Health Research and Development, BGI Genomics	0	1	0	0	0	1
3billion	0	1	0	0	0	1
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein	0	0	1	0	0	1
MVZ Medizinische Genetik Mainz	0	0	1	0	0	1

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