List of variants in gene DDX41 reported as benign by Genetic Services Laboratory, University of Chicago

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_016222.4(DDX41):c.*3C>T	rs73804364	0.00825
NM_016222.4(DDX41):c.1683C>T (p.Pro561=)	rs140652745	0.00703
NM_016222.4(DDX41):c.*74C>T	rs78923296	0.00457
NM_016222.4(DDX41):c.1233G>A (p.Glu411=)	rs147023941	0.00140
NM_016222.4(DDX41):c.139-4T>G	rs192297583	0.00127
NM_016222.4(DDX41):c.1354C>T (p.Leu452=)	rs143421709	0.00106
NM_016222.4(DDX41):c.1622-5C>G	rs374359854	0.00055
NM_016222.4(DDX41):c.1479C>T (p.Ser493=)	rs148853192	0.00026
NM_016222.4(DDX41):c.741G>A (p.Glu247=)	rs143274979	0.00019

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