Variants in gene DDX3X 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001356.5(DDX3X):c.104-10A>T	rs112766093	0.00708
NM_001356.5(DDX3X):c.969T>C (p.Thr323=)	rs368366114	0.00064
NM_001356.5(DDX3X):c.1616-3T>C	rs376431626	0.00030
NM_001356.5(DDX3X):c.1434G>A (p.Arg478=)	rs186110059	0.00026
NM_001356.5(DDX3X):c.1497+5G>A	rs201687537	0.00010
NM_001356.5(DDX3X):c.159C>T (p.Tyr53=)	rs370574418	0.00004
NM_001356.5(DDX3X):c.1593T>C (p.Arg531=)	rs761401204	0.00003
NM_001356.5(DDX3X):c.1095C>T (p.Val365=)	rs546763977	0.00002
NM_001356.5(DDX3X):c.1227C>T (p.Gly409=)	rs375797450	0.00002
NM_001356.5(DDX3X):c.1527T>C (p.Asn509=)	rs368642919	0.00002
NM_001356.5(DDX3X):c.1170+4C>T	rs745429365	0.00001
NM_001356.5(DDX3X):c.181A>G (p.Ser61Gly)	rs778806111	0.00001
NM_001356.5(DDX3X):c.1909+11T>C	rs772902981	0.00001
NM_001356.5(DDX3X):c.104-3dup	rs772419774
NM_001356.5(DDX3X):c.285-14_285-11del	rs751523291

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