Variants with conflicting interpretations "pathogenic" from Genomic Diagnostics Laboratory, National Institute of Medical Genomics and "uncertain significance" from any submitter

Minimum review status of the submission from Genomic Diagnostics Laboratory, National Institute of Medical Genomics:		Collection method of the submission from Genomic Diagnostics Laboratory, National Institute of Medical Genomics:
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_004082.5(DCTN1):c.212G>A (p.Gly71Glu)	rs67586389

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