List of variants in gene DDX41 reported as benign for DDX41-related hematologic malignancy predisposition syndrome

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_016222.4(DDX41):c.1200C>T (p.Arg400=)	rs335438	0.44246
NM_016222.4(DDX41):c.27+16G>C	rs112668086	0.03248
NM_016222.4(DDX41):c.1622-20C>G	rs73334184	0.01510
NM_016222.4(DDX41):c.1549+8C>T	rs145507265	0.01010
NM_016222.4(DDX41):c.27+2_27+5dup	rs142465759

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