Variants studied for Neurodegeneration with brain iron accumulation 8

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
1	1	8	2	2	1	13

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	not provided	total
CRAT	1	1	8	2	2	1	13

Submitter and significance breakdown #

Total submitters: 10

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	not provided	total
Revvity Omics, Revvity	0	0	2	0	0	0	2
Fulgent Genetics, Fulgent Genetics	0	0	0	2	0	0	2
Juno Genomics, Hangzhou Juno Genomics, Inc	0	0	2	0	0	0	2
Genome-Nilou Lab	0	0	0	0	2	0	2
Neuberg Centre For Genomic Medicine, NCGM	0	0	2	0	0	0	2
OMIM	1	0	0	0	0	0	1
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne	0	1	0	0	0	0	1
GenomeConnect, ClinGen	0	0	0	0	0	1	1
Pittsburgh Clinical Genomics Laboratory, University of Pittsburgh Medical Center	0	0	1	0	0	0	1
New York Genome Center	0	0	1	0	0	0	1

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