Variants in gene DDC with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001082971.2(DDC):c.1385G>A (p.Arg462Gln)	rs11575542	0.05076
NM_001082971.2(DDC):c.649A>G (p.Met217Val)	rs6263	0.03032
NM_001082971.2(DDC):c.629C>T (p.Pro210Leu)	rs6262	0.01372
NM_001082971.2(DDC):c.436-12T>C	rs144962948	0.00650
NM_001082971.2(DDC):c.96C>T (p.Asp32=)	rs11575290	0.00319
NM_001082971.2(DDC):c.550G>C (p.Val184Leu)	rs139433641	0.00011

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