List of variants in gene DNMT1 reported as uncertain significance for not specified

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:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001130823.3(DNMT1):c.301C>T (p.Arg101Trp)	rs369196079	0.00014
NM_001130823.3(DNMT1):c.382C>A (p.Pro128Thr)	rs146601335	0.00013
NM_001130823.3(DNMT1):c.3232G>A (p.Val1078Met)	rs560179619	0.00005
NM_001130823.3(DNMT1):c.2471C>T (p.Thr824Met)	rs140993011	0.00004
NM_001130823.3(DNMT1):c.2602G>A (p.Glu868Lys)	rs761717775	0.00003
NM_001130823.3(DNMT1):c.355A>G (p.Arg119Gly)	rs146516082	0.00001
NM_001130823.3(DNMT1):c.1492+3_1492+6del
NM_001130823.3(DNMT1):c.2092A>T (p.Ser698Cys)	rs1029809799
NM_001130823.3(DNMT1):c.3524-5G>T

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