Variants studied for Greenberg dysplasia

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
9	2	74	8	14	105

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
LBR	9	2	74	8	14	105

Submitter and significance breakdown #

Total submitters: 9

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	1	69	6	14	90
OMIM	7	0	0	0	0	7
Fulgent Genetics, Fulgent Genetics	0	0	2	2	0	4
Genome-Nilou Lab	0	0	0	0	3	3
MGZ Medical Genetics Center	0	0	2	0	0	2
Baylor-Hopkins Center for Mendelian Genomics, Johns Hopkins University School of Medicine	2	0	0	0	0	2
New York Genome Center	0	0	2	0	0	2
Medical Genetics Center, Maternal and Child Health Hospital of Hubei Province	1	1	0	0	0	2
Clinical Genetics and Genomics, Karolinska University Hospital	0	0	1	0	0	1

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