Variants in gene DNAAF1 with conflicting interpretations "likely pathogenic" and "pathogenic"

Submission 1 (likely pathogenic) minimum review status:		Submission 1 (likely pathogenic) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (pathogenic) 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_178452.6(DNAAF1):c.1528+2T>C	rs569633512	0.00001
NM_178452.6(DNAAF1):c.1300_1322del (p.Gly434fs)	rs745495583
NM_178452.6(DNAAF1):c.778C>T (p.Gln260Ter)	rs2087613070

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