List of variants in gene BRCA1 reported as likely benign by Pathway Genomics

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.1067A>G (p.Gln356Arg)	rs1799950	0.04695
NM_007294.4(BRCA1):c.3119G>A (p.Ser1040Asn)	rs4986852	0.01109
NM_007294.4(BRCA1):c.2458A>G (p.Lys820Glu)	rs56082113	0.00964
NM_007294.4(BRCA1):c.5468-10C>A	rs8176316	0.00464
NM_007294.4(BRCA1):c.557C>A (p.Ser186Tyr)	rs55688530	0.00301
NM_007294.4(BRCA1):c.4535G>T (p.Ser1512Ile)	rs1800744	0.00240
NM_007294.4(BRCA1):c.1137T>G (p.Ile379Met)	rs56128296	0.00158
NM_007294.4(BRCA1):c.3024G>A (p.Met1008Ile)	rs1800704	0.00065
NM_007294.4(BRCA1):c.5348T>C (p.Met1783Thr)	rs55808233	0.00058
NM_007294.4(BRCA1):c.571G>A (p.Val191Ile)	rs80357090	0.00021
NM_007294.4(BRCA1):c.1789G>A (p.Glu597Lys)	rs55650082	0.00019
NM_007294.4(BRCA1):c.823G>A (p.Gly275Ser)	rs8176153

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