Variants with conflicting interpretations "uncertain significance" from Michigan Medical Genetics Laboratories, University of Michigan and "likely benign" from any submitter

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.6803G>A (p.Arg2268Lys)	rs80358906	0.00020
NM_000059.4(BRCA2):c.9501+3A>T	rs61757642	0.00008
NM_000059.4(BRCA2):c.5985C>T (p.Asn1995=)	rs374620036	0.00005
NM_000059.4(BRCA2):c.67+4T>C	rs373546450	0.00001
NM_007294.4(BRCA1):c.3944C>G (p.Pro1315Arg)	rs80357500	0.00001
NM_000059.4(BRCA2):c.476-9dup	rs276174849
NM_007294.4(BRCA1):c.1983G>A (p.Arg661=)	rs869320788

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