Variants with conflicting interpretations "likely benign" from Service de Génétique Moléculaire, Hôpital Robert Debré and "likely pathogenic" from any submitter

Minimum review status of the submission from Service de Génétique Moléculaire, Hôpital Robert Debré:		Collection method of the submission from Service de Génétique Moléculaire, Hôpital Robert Debré:
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_001195553.2(DCX):c.-22-364C>T	rs761786389	0.00003
NM_002880.4(RAF1):c.1172G>T (p.Arg391Met)	rs587782972

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