List of variants in gene DVL3 reported as 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_004423.4(DVL3):c.231+261A>G	rs1709642	0.43730
NM_004423.4(DVL3):c.1198+132C>T	rs1709638	0.32356
NM_004423.4(DVL3):c.1049-64T>C	rs73185720	0.14646
NM_004423.4(DVL3):c.162-211G>A	rs73185718	0.11151
NM_004423.4(DVL3):c.1498+287C>T	rs73185721	0.10742
NM_004423.4(DVL3):c.1715-4A>C	rs116002660	0.02243
NM_004423.4(DVL3):c.1714+6G>A	rs147393618	0.01837
NM_004423.4(DVL3):c.161+167C>T	rs115460025	0.01820
NM_004423.4(DVL3):c.1049-26C>G	rs73884885

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