List of variants reported as likely benign for not specified by Department of Pathology and Molecular Medicine, Queen's University

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.2883G>A (p.Gln961=)	rs11571655	0.00097
NM_007294.4(BRCA1):c.522A>G (p.Gln174=)	rs765432756	0.00002
NM_000059.4(BRCA2):c.6953G>A (p.Arg2318Gln)	rs80358921	0.00001
NM_000059.4(BRCA2):c.8487+20C>T	rs1135401939
NM_007294.4(BRCA1):c.670+8C>T	rs80358050
NM_007294.4(BRCA1):c.81-14C>T	rs80358006

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