Variants with conflicting interpretations "likely pathogenic" from GeneID Lab - Advanced Molecular Diagnostics and "likely benign" from any submitter

Minimum review status of the submission from GeneID Lab - Advanced Molecular Diagnostics:		Collection method of the submission from GeneID Lab - Advanced Molecular Diagnostics:
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_033056.4(PCDH15):c.5347_5363del (p.Pro1783fs)	rs748086016

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