Variants studied for Autosomal dominant cerebellar ataxia, deafness and narcolepsy; Hereditary sensory neuropathy-deafness-dementia syndrome

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
0	0	19	8	1	1	29

Gene and significance breakdown #

Total genes and gene combinations: 2

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Gene or gene combination	uncertain significance	likely benign	benign	not provided	total
DNMT1	18	6	1	1	26
DNMT1, LOC126862853	1	2	0	0	3

Submitter and significance breakdown #

Total submitters: 4

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Submitter	uncertain significance	likely benign	benign	not provided	total
Fulgent Genetics, Fulgent Genetics	17	8	1	0	26
Mayo Clinic Laboratories, Mayo Clinic	1	0	0	0	1
New York Genome Center	1	0	0	0	1
GenomeConnect - Invitae Patient Insights Network	0	0	0	1	1

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