Variants with conflicting interpretations "pathogenic" from Biology Pathology Center, Lille University Hospital and "likely pathogenic" from any submitter

Minimum review status of the submission from Biology Pathology Center, Lille University Hospital:		Collection method of the submission from Biology Pathology Center, Lille University Hospital:
Minimum review status of the other submission:		Collection method of the other submission:
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_001369.3(DNAH5):c.6037C>T (p.Arg2013Ter)	rs1273352530
NM_181426.2(CCDC39):c.2226C>A (p.Tyr742Ter)	rs772219642

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