List of variants in gene DDX11 reported as benign for Warsaw breakage syndrome

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_030653.4(DDX11):c.2536+13G>A	rs3925641	0.53836
NM_030653.4(DDX11):c.2271+18G>A	rs10771803	0.53832
NM_030653.4(DDX11):c.2053-15C>T	rs7966272	0.53829
NM_030653.4(DDX11):c.2572G>A (p.Val858Ile)	rs1046457	0.53816
NM_030653.4(DDX11):c.684+8A>G	rs7308773	0.53493
NM_030653.4(DDX11):c.855T>C (p.Cys285=)	rs3881298	0.53406
NM_030653.4(DDX11):c.1983C>T (p.Leu661=)	rs1046456	0.53295
NM_030653.4(DDX11):c.880+16A>G	rs2075318	0.53242
NM_030653.4(DDX11):c.1699C>G (p.Gln567Glu)	rs2075322	0.52892
NM_030653.4(DDX11):c.639-10A>T	rs7308754	0.52325
NM_030653.4(DDX11):c.638+15G>A	rs4931428	0.47740

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