Variants studied for Imerslund-Grasbeck syndrome type 1; Proteinuria, chronic benign

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)

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
16	84	530	51	2	682

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	total
CUBN	16	82	517	51	2	667
CUBN, LOC129390143	0	1	7	0	0	8
CUBN, LOC126860871	0	1	6	0	0	7

Submitter and significance breakdown #

Total submitters: 5

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
Fulgent Genetics, Fulgent Genetics	15	78	528	51	2	674
First Genomix Gene Laboratory, Genetic Diagnostics Department	1	6	0	0	0	7
Department of Pathology and Laboratory Medicine, Sinai Health System	0	2	0	0	0	2
New York Genome Center	0	0	2	0	0	2
Laboratorio de Genética Hospitales Universitarios Virgen de las Nieves y Clínico San Cecilio (Granada, Spain), Hospitales Universitarios Virgen de las Nieves y Clínico San Cecilio (Granada, Spain)	0	1	0	0	0	1

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