Variants studied for Obesity due to prohormone convertase I 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
13	7	82	6	4	112

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
CAST, LOC101929710, PCSK1	13	7	82	6	4	112

Submitter and significance breakdown #

Total submitters: 15

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	0	76	6	4	86
OMIM	10	0	0	0	0	10
Baylor Genetics	0	0	2	0	0	2
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	0	0	2	0	0	2
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München	0	2	0	0	0	2
3billion, Medical Genetics	0	2	0	0	0	2
Molecular Endocrinology Laboratory, Christian Medical College	0	1	1	0	0	2
Revvity Omics, Revvity	1	0	0	0	0	1
Mendelics	0	0	1	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	1	0	0	1
Center for Molecular Medicine, Children’s Hospital of Fudan University	1	0	0	0	0	1
New York Genome Center	0	0	1	0	0	1
Lifecell International Pvt. Ltd	0	1	0	0	0	1
Aleixo Muise Laboratory, Hospital For Sick Children	1	0	0	0	0	1
Neuberg Centre For Genomic Medicine, NCGM	0	1	0	0	0	1

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