Variants studied for Hyperlipoproteinemia, type 1D

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
13	8	6	0	0	22

Gene and significance breakdown #

Total genes and gene combinations: 1

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	total
GPIHBP1	13	8	6	22

Submitter and significance breakdown #

Total submitters: 15

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Submitter	pathogenic	likely pathogenic	uncertain significance	total
OMIM	10	0	0	10
New York Genome Center	0	1	3	4
3billion	0	2	2	4
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	2	0	1	3
Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine	2	0	0	2
Institute of Human Genetics, University of Leipzig Medical Center	0	1	1	2
Neuberg Centre For Genomic Medicine, NCGM	0	1	1	2
Baylor Genetics	0	1	0	1
MGZ Medical Genetics Center	0	1	0	1
Mendelics	1	0	0	1
Hadassah Hebrew University Medical Center	0	1	0	1
Kasturba Medical College, Manipal, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India	0	1	0	1
Reproductive Health Research and Development, BGI Genomics	0	1	0	1
GBinsight Genetic Testing by GB HealthWatch, Genben Lifesciences Corporation	0	1	0	1
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital	0	0	1	1

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