Variants with conflicting interpretations "pathogenic" from Genetic Diagnostic Laboratory, University of Pennsylvania School of Medicine and "likely pathogenic" from any submitter

Minimum review status of the submission from Genetic Diagnostic Laboratory, University of Pennsylvania School of Medicine:		Collection method of the submission from Genetic Diagnostic Laboratory, University of Pennsylvania School of Medicine:
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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000321.3(RB1):c.-198G>A	rs387906521
NM_000321.3(RB1):c.1216-1G>A	rs587778831
NM_000321.3(RB1):c.1696-12T>G	rs1060503088
NM_000321.3(RB1):c.1960G>T (p.Val654Leu)
NM_000321.3(RB1):c.2134T>C (p.Cys712Arg)	rs137853296
NM_000321.3(RB1):c.32_63del (p.Ala11fs)	rs1593411974
NM_000321.3(RB1):c.373G>T (p.Glu125Ter)	rs1952457111
NM_000321.3(RB1):c.939G>A (p.Glu313=)	rs2138116702

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