List of variants in gene BRCA1 reported as benign by CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.1971A>G (p.Gln657=)	rs28897679	0.00707
NM_007294.4(BRCA1):c.5406+8T>C	rs55946644	0.00514
NM_007294.4(BRCA1):c.114G>A (p.Lys38=)	rs1800062	0.00233
NM_007294.4(BRCA1):c.21C>T (p.Arg7=)	rs149402012	0.00165
NM_007294.4(BRCA1):c.4600G>A (p.Val1534Met)	rs55815649	0.00145
NM_007294.4(BRCA1):c.2521C>T (p.Arg841Trp)	rs1800709	0.00137
NM_007294.4(BRCA1):c.591C>T (p.Cys197=)	rs1799965	0.00117
NM_007294.4(BRCA1):c.4883T>C (p.Met1628Thr)	rs4986854	0.00098
NM_007294.4(BRCA1):c.2733A>G (p.Gly911=)	rs1800740	0.00066
NM_007294.4(BRCA1):c.3024G>A (p.Met1008Ile)	rs1800704	0.00065
NM_007294.4(BRCA1):c.981A>G (p.Thr327=)	rs1800063	0.00065
NM_007294.4(BRCA1):c.2566T>C (p.Tyr856His)	rs80356892	0.00046
NM_007294.4(BRCA1):c.1911T>C (p.Thr637=)	rs62625305	0.00013
NM_007294.4(BRCA1):c.5252G>A (p.Arg1751Gln)	rs80357442	0.00004
NM_007294.4(BRCA1):c.441+18CTT[6]	rs147856441

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