List of variants in gene WBP11 reported as pathogenic for Vertebral, cardiac, tracheoesophageal, renal, and limb defects

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_016312.3(WBP11):c.1521dup (p.Arg508fs)
NM_016312.3(WBP11):c.1559dup (p.Gly521fs)	rs767139774
NM_016312.3(WBP11):c.280C>T (p.Arg94Ter)	rs1949900423
NM_016312.3(WBP11):c.688C>T (p.Arg230Ter)	rs1949866551

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