ClinVar Miner

List of variants in gene DDX11 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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_030653.4(DDX11):c.927G>C (p.Gln309His)	rs765283170	0.00004
NM_030653.4(DDX11):c.1841G>A (p.Arg614Gln)	rs757733914	0.00003

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