Variants in gene DNAH1 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely 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_015512.5(DNAH1):c.10636C>T (p.Arg3546Ter)	rs200416242	0.00005
NM_015512.5(DNAH1):c.7864C>T (p.Arg2622Ter)	rs368033879	0.00002
NM_015512.5(DNAH1):c.7676del (p.Val2559fs)	rs765417610	0.00001

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