Variants with conflicting interpretations "pathogenic" from Genetic Diagnostics Department, Viafet Genomics Laboratory and "likely pathogenic" from any submitter

Minimum review status of the submission from Genetic Diagnostics Department, Viafet Genomics Laboratory:		Collection method of the submission from Genetic Diagnostics Department, Viafet Genomics Laboratory:
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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000250.2(MPO):c.1705C>T (p.Arg569Trp)	rs119468010	0.00173
NM_000157.4(GBA1):c.1342G>C (p.Asp448His)	rs1064651	0.00020

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