Variants with conflicting interpretations "likely pathogenic" from Department of Genetic, Henri Mondor Hospital, Assistance Publique des Hôpitaux de Paris and "uncertain significance" from any submitter

Minimum review status of the submission from Department of Genetic, Henri Mondor Hospital, Assistance Publique des Hôpitaux de Paris:		Collection method of the submission from Department of Genetic, Henri Mondor Hospital, Assistance Publique des Hôpitaux de Paris:
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: 1

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HGVS	dbSNP	gnomAD frequency
NM_003126.4(SPTA1):c.6421C>T (p.Arg2141Trp)	rs41273519

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