List of variants in gene VANGL1 reported as likely benign for Caudal regression sequence

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_138959.3(VANGL1):c.*1183del	rs3841008	0.25316
NM_138959.3(VANGL1):c.*3762CAAA[2]	rs144395099
NM_138959.3(VANGL1):c.*4089del	rs138659832

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