List of variants reported as likely benign for Breast and/or ovarian cancer by Foulkes Cancer Genetics LDI, Lady Davis Institute for Medical Research

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.9976A>T (p.Lys3326Ter)	rs11571833	0.00597
NM_007294.4(BRCA1):c.2167A>G (p.Asn723Asp)	rs4986845	0.00209
NM_007294.4(BRCA1):c.2002C>T (p.Leu668Phe)	rs80357250	0.00011
NM_000059.4(BRCA2):c.5985C>T (p.Asn1995=)	rs374620036	0.00005
NM_000059.4(BRCA2):c.9275A>G (p.Tyr3092Cys)	rs80359195	0.00005
NM_000059.4(BRCA2):c.8010G>A (p.Ser2670=)	rs146430937	0.00003
NM_000059.4(BRCA2):c.7021C>T (p.Arg2341Cys)	rs41293505	0.00002
NM_007294.4(BRCA1):c.5074+6C>G	rs80358032	0.00002
NM_000059.4(BRCA2):c.4968A>G (p.Thr1656=)	rs1060504597	0.00001
NM_007294.4(BRCA1):c.5506G>A (p.Glu1836Lys)	rs80356942	0.00001
NM_007294.4(BRCA1):c.1441C>G (p.Leu481Val)	rs1397842308
NM_007294.4(BRCA1):c.1863T>C (p.His621=)	rs786201460
NM_007294.4(BRCA1):c.3113A>C (p.Glu1038Ala)	rs16941
NM_007294.4(BRCA1):c.4255G>C (p.Glu1419Gln)	rs80357309
NM_007294.4(BRCA1):c.4654T>C (p.Tyr1552His)	rs1265352633

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