Variants in gene DDX41 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 12

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HGVS	dbSNP	gnomAD frequency
NM_016222.4(DDX41):c.*3C>T	rs73804364	0.00825
NM_016222.4(DDX41):c.*74C>T	rs78923296	0.00457
NM_016222.4(DDX41):c.1299G>A (p.Pro433=)	rs61736556	0.00257
NM_016222.4(DDX41):c.1233G>A (p.Glu411=)	rs147023941	0.00140
NM_016222.4(DDX41):c.1354C>T (p.Leu452=)	rs143421709	0.00106
NM_016222.4(DDX41):c.1470C>T (p.Asp490=)	rs151018711	0.00096
NM_016222.4(DDX41):c.741G>A (p.Glu247=)	rs143274979	0.00019
NM_016222.4(DDX41):c.591G>A (p.Lys197=)	rs149122003	0.00018
NM_016222.4(DDX41):c.1203T>G (p.Ala401=)	rs556840837	0.00005
NM_016222.4(DDX41):c.882C>T (p.Cys294=)	rs550154951	0.00004
NM_016222.4(DDX41):c.935+9T>G	rs534811902	0.00004
NM_016222.4(DDX41):c.139-5C>T	rs200837781

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