ClinVar Miner

List of variants in gene DDX11 reported as pathogenic by Duke University Health System Sequencing Clinic, Duke University Health System

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_030653.4(DDX11):c.1763-1G>C	rs148856317	0.00024
NM_030653.4(DDX11):c.2230C>T (p.Gln744Ter)	rs776627170

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