Variants with conflicting interpretations "pathogenic" from Reutter Lab, Institute of Human Genetics, University Hospital Bonn and "likely benign" from any submitter

Minimum review status of the submission from Reutter Lab, Institute of Human Genetics, University Hospital Bonn:		Collection method of the submission from Reutter Lab, Institute of Human Genetics, University Hospital Bonn:
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_003413.4(ZIC3):c.49G>T (p.Gly17Cys)	rs147232392	0.00206

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