List of variants in gene DVL1 reported as likely pathogenic for autosomal dominant Robinow syndrome

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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_001330311.2(DVL1):c.1571_1583del (p.Pro524fs)	rs1553173420
NM_001330311.2(DVL1):c.1682_1683dup (p.Ser562fs)	rs1643642110
NM_001330311.2(DVL1):c.1715-1G>A	rs2100704859
NM_001330311.2(DVL1):c.363-1G>C

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