Variants in gene ZEB2 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_014795.4(ZEB2):c.2084G>A (p.Arg695Gln)	rs147693839	0.00012
NM_014795.4(ZEB2):c.219C>T (p.His73=)	rs778851716	0.00005
NM_014795.4(ZEB2):c.220G>A (p.Val74Met)	rs767169568	0.00002
NM_014795.4(ZEB2):c.2766A>T (p.Pro922=)	rs185223937	0.00002
NM_014795.4(ZEB2):c.179C>T (p.Thr60Met)	rs780890592	0.00001
NM_014795.4(ZEB2):c.2004G>T (p.Glu668Asp)	rs767506087	0.00001
NM_014795.4(ZEB2):c.2497A>G (p.Thr833Ala)	rs1490526407	0.00001
NM_014795.4(ZEB2):c.26G>A (p.Gly9Asp)	rs1242134764	0.00001
NM_014795.4(ZEB2):c.385G>A (p.Ala129Thr)	rs730881187	0.00001
NM_014795.4(ZEB2):c.1446A>C (p.Glu482Asp)	rs886043609
NM_014795.4(ZEB2):c.1542G>T (p.Pro514=)	rs141674976
NM_014795.4(ZEB2):c.2471T>C (p.Met824Thr)	rs1553961536
NM_014795.4(ZEB2):c.3535A>G (p.Ile1179Val)	rs1360979536
NM_014795.4(ZEB2):c.74-3C>T	rs984545941
NM_014795.4(ZEB2):c.807+3G>T	rs144925893
NM_014795.4(ZEB2):c.9G>A (p.Gln3=)	rs149882004

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