List of variants in gene DVL3 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_004423.4(DVL3):c.1473C>G (p.Tyr491Ter)	rs2109022762
NM_004423.4(DVL3):c.1617del (p.Gln539fs)	rs1553811652
NM_004423.4(DVL3):c.1715-1G>A	rs869025217
NM_004423.4(DVL3):c.1715-1G>C	rs869025217
NM_004423.4(DVL3):c.1715-2del	rs2109023862
NM_004423.4(DVL3):c.292del (p.Glu98fs)

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