List of variants in gene ZEB2 reported as benign by Genetic Services Laboratory, University of Chicago

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_014795.4(ZEB2):c.930C>T (p.Tyr310=)	rs6711223	0.01102
NM_014795.4(ZEB2):c.2141C>T (p.Pro714Leu)	rs112581563	0.00281
NM_014795.4(ZEB2):c.489C>T (p.Ile163=)	rs138859323	0.00277
NM_014795.4(ZEB2):c.1480C>T (p.Pro494Ser)	rs144952836	0.00206
NM_014795.4(ZEB2):c.3471C>T (p.Asp1157=)	rs149526010	0.00186
NM_014795.4(ZEB2):c.2230A>G (p.Ile744Val)	rs112005830	0.00087
NM_014795.4(ZEB2):c.798G>C (p.Gly266=)	rs34961586	0.00078
NM_014795.4(ZEB2):c.1276T>A (p.Leu426Ile)	rs201881288	0.00036
NM_014795.4(ZEB2):c.1438G>T (p.Ala480Ser)	rs143854197	0.00026
NM_014795.4(ZEB2):c.1735A>G (p.Thr579Ala)	rs140593583	0.00026
NM_014795.4(ZEB2):c.2142G>A (p.Pro714=)	rs201180901	0.00025
NM_014795.4(ZEB2):c.462G>A (p.Glu154=)	rs372940559	0.00023
NM_014795.4(ZEB2):c.2203C>T (p.Pro735Ser)	rs144154908	0.00001
NM_014795.4(ZEB2):c.1410T>A (p.Thr470=)	rs34890427
NM_014795.4(ZEB2):c.9G>C (p.Gln3His)	rs149882004

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