List of variants in gene BRCA1 reported as likely pathogenic by Research Molecular Genetics Laboratory, Women's College Hospital, University of Toronto

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.116G>A (p.Cys39Tyr)	rs80357498	0.00003
NM_007294.4(BRCA1):c.212+3A>G	rs80358083	0.00001
NM_007294.4(BRCA1):c.5096G>A (p.Arg1699Gln)	rs41293459	0.00001
NM_007294.4(BRCA1):c.131G>T (p.Cys44Phe)	rs80357446
NM_007294.4(BRCA1):c.4986+3G>C	rs80358023
NM_007294.4(BRCA1):c.5074G>A (p.Asp1692Asn)	rs80187739
NM_007294.4(BRCA1):c.5207T>C (p.Val1736Ala)	rs45553935

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