List of variants in gene DDX3X reported as likely benign by GeneDx

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: 29

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HGVS	dbSNP	gnomAD frequency
NM_001356.5(DDX3X):c.-72G>A	rs145191840	0.01257
NM_001356.5(DDX3X):c.544-71T>G	rs141846961	0.00897
NM_001356.5(DDX3X):c.104-10A>T	rs112766093	0.00708
NM_001356.5(DDX3X):c.766-84A>G	rs12011185	0.00572
NM_001356.5(DDX3X):c.45+316T>G	rs145059861	0.00521
NM_001356.5(DDX3X):c.1026-89T>A	rs146259535	0.00473
NM_001356.5(DDX3X):c.284+72T>G	rs146299715	0.00426
NM_001356.5(DDX3X):c.151+103T>G	rs144446471	0.00373
NM_001356.5(DDX3X):c.152-54A>G	rs183722470	0.00330
NM_001356.5(DDX3X):c.1497+29A>G	rs190934026	0.00324
NM_001356.5(DDX3X):c.1497+46T>C	rs2272173	0.00049
NM_001356.5(DDX3X):c.1434G>A (p.Arg478=)	rs186110059	0.00026
NM_001356.5(DDX3X):c.1593T>C (p.Arg531=)	rs761401204	0.00011
NM_001356.5(DDX3X):c.1497+5G>A	rs201687537	0.00010
NM_001356.5(DDX3X):c.426A>C (p.Pro142=)	rs779721240	0.00010
NM_001356.5(DDX3X):c.966C>T (p.Ala322=)	rs374463509	0.00005
NM_001356.5(DDX3X):c.159C>T (p.Tyr53=)	rs370574418	0.00004
NM_001356.5(DDX3X):c.1315+5C>T	rs368731454	0.00002
NM_001356.5(DDX3X):c.251T>G (p.Phe84Cys)	rs892274119	0.00002
NM_001356.5(DDX3X):c.1316-7A>T	rs781749765	0.00001
NM_001356.5(DDX3X):c.1527T>C (p.Asn509=)	rs368642919	0.00001
NM_001356.5(DDX3X):c.1025+24_1025+28del	rs200111332
NM_001356.5(DDX3X):c.103+193dup	rs5902274
NM_001356.5(DDX3X):c.104-3dup	rs772419774
NM_001356.5(DDX3X):c.104-4_104-3dup	rs772419774
NM_001356.5(DDX3X):c.285-14_285-11del	rs751523291
NM_001356.5(DDX3X):c.675A>G (p.Gln225=)	rs1057522471
NM_001356.5(DDX3X):c.680-174_680-173del	rs72460118
NM_001356.5(DDX3X):c.766-11T>C	rs1555953395

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