List of variants reported as likely benign for Breast and/or ovarian cancer by CSER _CC_NCGL, University of Washington

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.6347A>G (p.His2116Arg)	rs55953736	0.00396
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_007294.4(BRCA1):c.5005G>T (p.Ala1669Ser)	rs80357087	0.00019

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