List of variants in gene DNMT1 reported as benign 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_001130823.3(DNMT1):c.206G>A (p.Arg69His)	rs61750053	0.01134
NM_001130823.3(DNMT1):c.3939C>T (p.Gly1313=)	rs142903301	0.00977
NM_001130823.3(DNMT1):c.1095C>T (p.His365=)	rs116502459	0.00699
NM_001130823.3(DNMT1):c.1500C>T (p.Ala500=)	rs75443147	0.00552
NM_001130823.3(DNMT1):c.4294-17C>A	rs79585069	0.00551
NM_001130823.3(DNMT1):c.4294-19G>C	rs2290683	0.00551
NM_001130823.3(DNMT1):c.2382-4C>T	rs74505694	0.00548
NM_001130823.3(DNMT1):c.2463C>T (p.Leu821=)	rs61750051	0.00377
NM_001130823.3(DNMT1):c.4428T>G (p.His1476Gln)	rs142647321	0.00251
NM_001130823.3(DNMT1):c.1944C>T (p.Phe648=)	rs61750052	0.00249
NM_001130823.3(DNMT1):c.2117+13G>A	rs112660071	0.00153
NM_001130823.3(DNMT1):c.731G>A (p.Gly244Glu)	rs150999369	0.00066
NM_001130823.3(DNMT1):c.1722G>A (p.Val574=)	rs140376680	0.00006
NM_001130823.3(DNMT1):c.4860C>T (p.Ala1620=)	rs576877219	0.00001

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