Variants in gene DNAAF1 with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (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: 5

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HGVS	dbSNP	gnomAD frequency
NM_178452.6(DNAAF1):c.1354C>A (p.Pro452Thr)	rs145680314	0.00085
NM_178452.6(DNAAF1):c.546C>G (p.Asn182Lys)	rs144018942	0.00080
NM_178452.6(DNAAF1):c.1988C>T (p.Pro663Leu)	rs147393144	0.00053
NM_178452.6(DNAAF1):c.1698+1G>A	rs139519641	0.00041
NM_178452.6(DNAAF1):c.1645-19G>A	rs192432193	0.00024

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