List of variants in gene BRCA1 reported as uncertain significance by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.-19-22A>G	rs774892235	0.00003
NM_007294.4(BRCA1):c.1555A>C (p.Lys519Gln)	rs397508882	0.00001
NM_007294.4(BRCA1):c.4484G>A (p.Arg1495Lys)	rs80357389
NM_007294.4(BRCA1):c.5467+3A>C	rs431825417
NM_007294.4(BRCA1):c.5495T>G (p.Val1832Gly)	rs749290001
NM_007294.4(BRCA1):c.670G>C (p.Ala224Pro)	rs431825419

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