List of variants in gene DVL3 reported as likely benign by GeneDx

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_004423.4(DVL3):c.162-203A>G	rs138493584	0.02596
NM_004423.4(DVL3):c.763+287C>T	rs77851575	0.01949
NM_004423.4(DVL3):c.232-211C>T	rs73185719	0.01040
NM_004423.4(DVL3):c.764-194T>C	rs73045935	0.00628
NM_004423.4(DVL3):c.291G>A (p.Ser97=)	rs150288196	0.00484
NM_004423.4(DVL3):c.1199-156C>G	rs79715240

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