Variants studied for focal segmental glomerulosclerosis 3, susceptibility to

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
4	4	72	19	36	133

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	benign	total
CD2AP	4	4	67	19	31	123
CD2AP, CD2AP-DT, LOC129996604	0	0	5	0	5	10

Submitter and significance breakdown #

Total submitters: 12

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Illumina Laboratory Services, Illumina	0	0	56	6	36	98
Fulgent Genetics, Fulgent Genetics	3	1	11	14	0	29
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare	1	1	3	0	0	5
Baylor Genetics	0	0	2	0	0	2
Revvity Omics, Revvity	0	0	2	0	0	2
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	0	1	1	0	0	2
Genome Diagnostics Laboratory, University Medical Center Utrecht	0	0	0	0	1	1
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	1	0	0	0	1
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen	0	0	0	0	1	1
3billion	1	0	0	0	0	1
Molecular Genetics, Royal Melbourne Hospital	0	0	1	0	0	1
MVZ Medizinische Genetik Mainz	0	1	0	0	0	1

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