Variants studied for familial apolipoprotein C-II deficiency

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
12	0	18	4	8	39

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	uncertain significance	likely benign	benign	total
APOC2, APOC4-APOC2	12	18	4	8	39

Submitter and significance breakdown #

Total submitters: 10

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Submitter	pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	13	2	8	23
OMIM	9	0	0	0	9
Fulgent Genetics, Fulgent Genetics	1	0	2	0	3
New York Genome Center	0	3	0	0	3
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	1	1	0	0	2
Reproductive Health Research and Development, BGI Genomics	0	1	0	1	2
Centogene AG - the Rare Disease Company	0	1	0	0	1
Mendelics	1	0	0	0	1
Genomic Research Center, Shahid Beheshti University of Medical Sciences	1	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	1	0	0	1

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