ClinVar Miner

List of variants in gene combination DNMT1, LOC126862853 reported as likely benign 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001130823.3(DNMT1):c.4656+9G>A	rs367724672	0.00061
NM_001130823.3(DNMT1):c.4773+11C>T	rs777602633	0.00003

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