Variants studied for focal segmental glomerulosclerosis 6

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	not provided	total
5	12	160	29	6	1	212

Gene and significance breakdown #

Total genes and gene combinations: 3

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
MYO1E	5	12	153	27	6	1	203
LOC112272600, MYO1E	0	0	7	1	0	0	8
LDHAL6B, MYO1E	0	0	0	1	0	0	1

Submitter and significance breakdown #

Total submitters: 14

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Fulgent Genetics, Fulgent Genetics	1	10	151	28	3	0	193
Baylor Genetics	0	0	3	0	0	0	3
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre	1	0	2	0	0	0	3
Genome-Nilou Lab	0	0	0	0	3	0	3
Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein	0	0	3	0	0	0	3
OMIM	2	0	0	0	0	0	2
Molecular Biology Laboratory, Fundació Puigvert	1	1	0	0	0	0	2
Revvity Omics, Revvity	0	0	1	0	0	0	1
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München	0	1	0	0	0	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	0	1	0	0	0	1
Department of Pathology and Laboratory Medicine, Sinai Health System	0	0	1	0	0	0	1
GenomeConnect, ClinGen	0	0	0	0	0	1	1
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital	0	0	0	1	0	0	1
MVZ Medizinische Genetik Mainz	0	0	1	0	0	0	1

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