List of variants in gene DDX41 reported as pathogenic for hematologic disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_016222.4(DDX41):c.3G>A (p.Met1Ile)	rs141601766	0.00012
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.155dup (p.Arg53fs)	rs766117035
NM_016222.4(DDX41):c.1621+5G>T	rs2127435833
NM_016222.4(DDX41):c.370C>T (p.Arg124Ter)	rs1297703150
NM_016222.4(DDX41):c.719delinsCG (p.Ile240fs)	rs1761157695

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