List of variants reported as likely benign for breast disorder by CSER _CC_NCGL, University of Washington

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Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_004360.5(CDH1):c.1774G>A (p.Ala592Thr)	rs35187787	0.00311
NM_000059.4(BRCA2):c.5640T>G (p.Asn1880Lys)	rs11571657	0.00288
NM_000059.4(BRCA2):c.6323G>A (p.Arg2108His)	rs35029074	0.00260
NM_000059.4(BRCA2):c.8182G>A (p.Val2728Ile)	rs28897749	0.00239
NM_000059.4(BRCA2):c.7150C>A (p.Gln2384Lys)	rs55977008	0.00203
NM_000059.4(BRCA2):c.1792A>G (p.Thr598Ala)	rs28897710	0.00182
NM_007294.4(BRCA1):c.1137T>G (p.Ile379Met)	rs56128296	0.00158
NM_007294.4(BRCA1):c.4682C>T (p.Thr1561Ile)	rs56158747	0.00150
NM_007294.4(BRCA1):c.4883T>C (p.Met1628Thr)	rs4986854	0.00098
NM_000059.4(BRCA2):c.978C>A (p.Ser326Arg)	rs28897706	0.00082
NM_000059.4(BRCA2):c.1514T>C (p.Ile505Thr)	rs28897708	0.00074
NM_007294.4(BRCA1):c.4691T>C (p.Leu1564Pro)	rs56119278	0.00059
NM_007294.4(BRCA1):c.2566T>C (p.Tyr856His)	rs80356892	0.00046
NM_000059.4(BRCA2):c.223G>C (p.Ala75Pro)	rs28897701	0.00032
NM_007294.4(BRCA1):c.1648A>C (p.Asn550His)	rs56012641	0.00029
NM_000059.4(BRCA2):c.1786G>C (p.Asp596His)	rs56328701	0.00025
NM_000059.4(BRCA2):c.9038C>T (p.Thr3013Ile)	rs28897755	0.00022
NM_000059.4(BRCA2):c.5710C>G (p.Leu1904Val)	rs55875643	0.00020
NM_007294.4(BRCA1):c.3748G>A (p.Glu1250Lys)	rs28897686	0.00017
NM_000059.4(BRCA2):c.4061C>T (p.Thr1354Met)	rs80358656	0.00014
NM_000059.4(BRCA2):c.3055C>G (p.Leu1019Val)	rs55638633	0.00012
NM_000059.4(BRCA2):c.10045A>G (p.Thr3349Ala)	rs80358387	0.00010
NM_007294.4(BRCA1):c.314A>G (p.Tyr105Cys)	rs28897673	0.00009
NM_000059.4(BRCA2):c.1662T>G (p.Cys554Trp)	rs80358451	0.00006
NM_000059.4(BRCA2):c.3032C>G (p.Thr1011Arg)	rs80358548	0.00004
NM_000059.4(BRCA2):c.9586A>G (p.Lys3196Glu)	rs80359228	0.00004
NM_007294.4(BRCA1):c.3657G>C (p.Glu1219Asp)	rs80356876	0.00002

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