List of variants in gene DNMT1 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001130823.3(DNMT1):c.575C>T (p.Ala192Val)	rs62621089	0.00023
NM_001130823.3(DNMT1):c.4876G>A (p.Glu1626Lys)	rs201774098	0.00011
NM_001130823.3(DNMT1):c.868G>A (p.Glu290Lys)	rs200024502	0.00011
NM_001130823.3(DNMT1):c.1043C>T (p.Pro348Leu)	rs370592431	0.00009
NM_001130823.3(DNMT1):c.4193C>T (p.Ser1398Leu)	rs375225009	0.00001
NM_001130823.3(DNMT1):c.2092A>T (p.Ser698Cys)	rs1029809799
NM_001130823.3(DNMT1):c.950A>G (p.Glu317Gly)	rs1478185698

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