List of variants in gene DNMT1 reported as likely benign for Autosomal dominant cerebellar ataxia, deafness and narcolepsy; Hereditary sensory neuropathy-deafness-dementia syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001130823.3(DNMT1):c.2463C>T (p.Leu821=)	rs61750051	0.00377
NM_001130823.3(DNMT1):c.731G>A (p.Gly244Glu)	rs150999369	0.00066
NM_001130823.3(DNMT1):c.1224C>T (p.Asn408=)	rs199584370	0.00035
NM_001130823.3(DNMT1):c.3711C>T (p.Cys1237=)	rs139909192	0.00010
NM_001130823.3(DNMT1):c.1986C>T (p.Asn662=)	rs377704053	0.00007
NM_001130823.3(DNMT1):c.3999C>T (p.Ala1333=)	rs747144567	0.00002

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