List of variants in gene DNMT1 reported as benign for autosomal dominant cerebellar ataxia, deafness and narcolepsy

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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.1782A>G (p.Thr594=)	rs721186	0.99062
NM_001130823.3(DNMT1):c.1832+14A>G	rs2114724	0.50847
NM_001130823.3(DNMT1):c.1389A>G (p.Pro463=)	rs2228611	0.50821
NM_001130823.3(DNMT1):c.3394+34T>C	rs2290684	0.49102
NM_001130823.3(DNMT1):c.2721-45C>T	rs2288349	0.35077
NM_001130823.3(DNMT1):c.1044-8del	rs59599980

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