Variants in gene DNAAF2 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_018139.3(DNAAF2):c.1953A>G (p.Pro651=)	rs34352773	0.00287
NM_018139.3(DNAAF2):c.731C>A (p.Ala244Glu)	rs112700048	0.00068
NM_018139.3(DNAAF2):c.263G>A (p.Cys88Tyr)	rs549457480	0.00056
NM_018139.3(DNAAF2):c.1595A>G (p.Glu532Gly)	rs143210369	0.00052
NM_018139.3(DNAAF2):c.824C>T (p.Ala275Val)	rs200291432	0.00014
NM_018139.3(DNAAF2):c.1969C>T (p.Leu657Phe)	rs187863107	0.00008

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