List of variants in gene ZEB2 reported as uncertain significance by Eurofins NTD LLC (GA)

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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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.3219C>T (p.His1073=)	rs139944383	0.00009
NM_014795.4(ZEB2):c.219C>T (p.His73=)	rs778851716	0.00005
NM_014795.4(ZEB2):c.374C>T (p.Thr125Met)	rs727504227	0.00004
NM_014795.4(ZEB2):c.2886+4A>C	rs754532627	0.00003
NM_014795.4(ZEB2):c.403+9T>C	rs886042422	0.00003
NM_014795.4(ZEB2):c.2766A>T (p.Pro922=)	rs185223937	0.00002
NM_014795.4(ZEB2):c.1877G>A (p.Gly626Glu)	rs794727923	0.00001
NM_014795.4(ZEB2):c.773G>A (p.Arg258Gln)	rs730881173	0.00001
NM_014795.4(ZEB2):c.1446A>C (p.Glu482Asp)	rs886043609
NM_014795.4(ZEB2):c.1542G>A (p.Pro514=)	rs141674976
NM_014795.4(ZEB2):c.1542G>T (p.Pro514=)	rs141674976
NM_014795.4(ZEB2):c.1927_1934delinsGG (p.Lys643_Met645delinsGly)	rs796065335
NM_014795.4(ZEB2):c.2281A>T (p.Thr761Ser)	rs867243713
NM_014795.4(ZEB2):c.2641A>C (p.Asn881His)	rs794727922
NM_014795.4(ZEB2):c.3077_3079del (p.Pro1026del)	rs398124279
NM_014795.4(ZEB2):c.9G>A (p.Gln3=)	rs149882004

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