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

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001130823.3(DNMT1):c.1520C>T (p.Pro507Leu)	rs1599366542
NM_001130823.3(DNMT1):c.1531T>C (p.Tyr511His)	rs199473692
NM_001130823.3(DNMT1):c.1532A>G (p.Tyr511Cys)	rs199473690
NM_001130823.3(DNMT1):c.1709C>T (p.Ala570Val)	rs397509392

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