Variants studied for congenital stationary night blindness 1B

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
10	4	3	4	9	30

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
GRM6, ZNF454	6	2	2	3	8	21
GRM6	4	1	1	1	1	8
GPR179	0	1	0	0	0	1

Submitter and significance breakdown #

Total submitters: 12

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Submitter	pathogenic	likely pathogenic	uncertain significance	likely benign	benign	total
OMIM	8	0	0	0	0	8
Genome-Nilou Lab	0	0	0	0	8	8
Revvity Omics, Revvity	2	1	1	0	0	4
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center	0	0	0	2	1	3
Fulgent Genetics, Fulgent Genetics	0	0	0	2	0	2
Neuberg Centre For Genomic Medicine, NCGM	0	2	0	0	0	2
MGZ Medical Genetics Center	0	1	0	0	0	1
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center	0	1	0	0	0	1
Soonchunhyang University Bucheon Hospital, Soonchunhyang University Medical Center	0	0	1	0	0	1
Ocular Genomics Institute, Massachusetts Eye and Ear	0	0	1	0	0	1
Génétique des Maladies du Développement, Hospices Civils de Lyon	1	0	0	0	0	1
3billion	1	0	0	0	0	1

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