Variants in gene DNMT1 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 7

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HGVS	dbSNP	gnomAD frequency
NM_001130823.3(DNMT1):c.150C>T (p.His50=)	rs146112081	0.00182
NM_001130823.3(DNMT1):c.406C>T (p.Arg136Cys)	rs138841970	0.00024
NM_001130823.3(DNMT1):c.575C>T (p.Ala192Val)	rs62621089	0.00023
NM_001130823.3(DNMT1):c.382C>A (p.Pro128Thr)	rs146601335	0.00013
NM_001130823.3(DNMT1):c.3806+6C>T	rs371779379	0.00006
NM_001130823.3(DNMT1):c.3668G>A (p.Arg1223His)	rs757460628	0.00001
NM_001130823.3(DNMT1):c.3948+4G>A	rs774356396

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