List of variants in gene combination DVL2, LOC126862480 reported as likely benign

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004422.3(DVL2):c.579G>A (p.Glu193=)	rs146424893	0.00054
NM_004422.3(DVL2):c.332C>T (p.Ala111Val)	rs371764720	0.00023
NM_004422.3(DVL2):c.656+8T>G	rs940773303	0.00001

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