Variants with conflicting interpretations "likely benign" from Michigan Medical Genetics Laboratories, University of Michigan and "benign" from Sharing Clinical Reports Project (SCRP)

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.5640T>G (p.Asn1880Lys)	rs11571657	0.00288
NM_000059.4(BRCA2):c.5768A>C (p.Asp1923Ala)	rs45491005	0.00088
NM_000059.4(BRCA2):c.1514T>C (p.Ile505Thr)	rs28897708	0.00074
NM_000059.4(BRCA2):c.4585G>A (p.Gly1529Arg)	rs28897728	0.00044
NM_007294.4(BRCA1):c.3708T>G (p.Asn1236Lys)	rs28897687	0.00031
NM_000059.4(BRCA2):c.506A>G (p.Lys169Arg)	rs80358730	0.00008
NM_000059.4(BRCA2):c.2320A>G (p.Thr774Ala)	rs55968715	0.00006
NM_000059.4(BRCA2):c.750G>A (p.Val250=)	rs143214959	0.00005
NM_007294.4(BRCA1):c.425C>A (p.Pro142His)	rs55971303	0.00004
NM_007294.4(BRCA1):c.2447A>G (p.His816Arg)	rs80357108	0.00003
NM_000059.4(BRCA2):c.4928T>C (p.Val1643Ala)	rs28897731

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