Variants with conflicting interpretations "pathogenic" from Familial Cancer Clinical Unit, Spanish National Cancer Research Centre (CNIO) and "likely pathogenic" from any submitter

Minimum review status of the submission from Familial Cancer Clinical Unit, Spanish National Cancer Research Centre (CNIO):		Collection method of the submission from Familial Cancer Clinical Unit, Spanish National Cancer Research Centre (CNIO):
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_004360.5(CDH1):c.1679C>G (p.Thr560Arg)	rs746481984

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