ClinVar Miner

List of variants in gene DDX41 reported as pathogenic for acute disease

Included ClinVar conditions (75):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_016222.4(DDX41):c.415_418dup (p.Asp140delinsGlyTer) rs762890562 0.00007
NM_016222.4(DDX41):c.931C>T (p.Arg311Ter) rs899399494 0.00001
NM_016222.3:c.[711G>T;712C>A]
NM_016222.4(DDX41):c.719delinsCG (p.Ile240fs) rs1761157695

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