List of variants in gene DVL3 reported as uncertain significance for Autosomal dominant Robinow syndrome 3

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_004423.4(DVL3):c.808G>A (p.Glu270Lys)	rs1714576025	0.00001
NM_004423.4(DVL3):c.950G>A (p.Arg317Gln)	rs749840241	0.00001
NM_004423.4(DVL3):c.1120G>A (p.Ala374Thr)	rs1714612048
NM_004423.4(DVL3):c.1552C>T (p.Gln518Ter)
NM_004423.4(DVL3):c.1738C>T (p.Arg580Cys)	rs2473705740
NM_004423.4(DVL3):c.190A>T (p.Asn64Tyr)
NM_004423.4(DVL3):c.1947_1950del (p.His650fs)
NM_004423.4(DVL3):c.1949_1950del (p.His650fs)	rs2473706145
NM_004423.4(DVL3):c.706A>G (p.Ser236Gly)	rs1714548192
NM_004423.4(DVL3):c.883C>G (p.Pro295Ala)
NM_004423.4(DVL3):c.899T>C (p.Leu300Ser)
NM_004423.4(DVL3):c.903G>C (p.Gln301His)	rs2473700274

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