Variants in gene DDX41 with conflicting interpretations "risk factor" and "uncertain significance"

Submission 1 (risk factor) minimum review status:		Submission 1 (risk factor) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_016222.4(DDX41):c.490C>T (p.Arg164Trp)	rs142143752	0.00017
NM_016222.4(DDX41):c.3G>A (p.Met1Ile)	rs141601766	0.00012

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