Variants studied for Autosomal dominant cerebellar ataxia, deafness and narcolepsy

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	8	0	6	21

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	pathogenic	likely pathogenic	uncertain significance	benign	total
DNMT1	4	3	6	6	18
DNMT1, LOC126862853	0	1	2	0	3

Submitter and significance breakdown #

Total submitters: 12

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Submitter	pathogenic	likely pathogenic	uncertain significance	benign	total
Genome-Nilou Lab	0	0	0	6	6
OMIM	3	0	0	0	3
Baylor Genetics	0	0	2	0	2
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München	0	2	0	0	2
Centre for Mendelian Genomics, University Medical Centre Ljubljana	0	0	2	0	2
Neuberg Centre For Genomic Medicine, NCGM	0	0	2	0	2
Mendelics	0	1	0	0	1
Victorian Clinical Genetics Services, Murdoch Childrens Research Institute	0	0	1	0	1
Genomic Research Center, Shahid Beheshti University of Medical Sciences	0	0	1	0	1
Institute of Human Genetics, University of Leipzig Medical Center	0	1	0	0	1
Molecular Medicine for Neurodegenerative and Neuromuscular Diseases Unit, IRCCS Fondazione Stella Maris	1	0	0	0	1
3billion	1	0	0	0	1

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