Variants with conflicting interpretations "uncertain significance" from Michigan Medical Genetics Laboratories, University of Michigan and "likely benign" from Genome Diagnostics Laboratory, University Medical Center Utrecht

Minimum review status of the submission from Michigan Medical Genetics Laboratories, University of Michigan:		Collection method of the submission from Michigan Medical Genetics Laboratories, University of Michigan:
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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.9501+3A>T	rs61757642	0.00007
NM_000059.4(BRCA2):c.67+4T>C	rs373546450	0.00001
NM_000059.4(BRCA2):c.476-9dup	rs276174849

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