ClinVar Miner

List of variants in gene DVL3 reported as uncertain significance by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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)
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Total variants: 2

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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.903G>C (p.Gln301His)	rs2473700274

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