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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001082971.2(DDC):c.715A>T (p.Met239Leu)	rs11575376	0.00069
NM_001082971.2(DDC):c.1435A>G (p.Arg479Gly)	rs200450773	0.00016
NM_001082971.2(DDC):c.366C>T (p.Leu122=)	rs377528325	0.00014
NM_001082971.2(DDC):c.315+11G>A	rs753275419	0.00006
NM_001082971.2(DDC):c.816A>C (p.Ala272=)	rs767990522	0.00006
NM_001082971.2(DDC):c.1044T>C (p.His348=)	rs527805112	0.00004
NM_001082971.2(DDC):c.316-6C>T	rs377474761	0.00004
NM_001082971.2(DDC):c.822C>T (p.Tyr274=)	rs746729797	0.00004
NM_001082971.2(DDC):c.6C>T (p.Asn2=)	rs749246611	0.00003
NM_001082971.2(DDC):c.564C>T (p.Ser188=)	rs371336321	0.00001
NM_001082971.2(DDC):c.1041+12A>T	rs2042651349
NM_001082971.2(DDC):c.316-5G>C	rs2044474558
NM_001082971.2(DDC):c.436-6A>G	rs770694855

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