List of variants in gene DVL3 reported as 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004423.4(DVL3):c.1585del (p.Ala529fs)	rs869025215
NM_004423.4(DVL3):c.1592del (p.Pro531fs)	rs1577052471
NM_004423.4(DVL3):c.1715-1G>A	rs869025217
NM_004423.4(DVL3):c.1715-2A>C	rs869025216
NM_004423.4(DVL3):c.1715-2A>G	rs869025216
NM_004423.4(DVL3):c.1716del (p.Ser573fs)	rs869025218
NM_004423.4(DVL3):c.1749del (p.Ser583fs)	rs869025219
NM_004423.4(DVL3):c.1751_1754del (p.Asp584fs)	rs1577052785

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