List of variants reported as benign by Hereditary Cancer Genetics group, Vall d'Hebron Institute of Oncology

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.4113G>A (p.Gly1371=)	rs147448807	0.00150
NM_000059.4(BRCA2):c.7435+6G>A	rs81002852	0.00053
NM_007294.4(BRCA1):c.4358-10C>T	rs80358111	0.00024
NM_000059.4(BRCA2):c.7805+13A>G	rs149769332	0.00019
NM_000059.4(BRCA2):c.9501+9A>C	rs81002867	0.00011
NM_000059.4(BRCA2):c.632-16A>C	rs81002905	0.00003
NM_007294.4(BRCA1):c.5333-8C>T	rs80358084	0.00003
NM_000059.4(BRCA2):c.9501+4A>G	rs81002848	0.00002
NM_007294.4(BRCA1):c.5074+6C>G	rs80358032	0.00002
NM_007294.4(BRCA1):c.4485-10A>G	rs863224420	0.00001
NM_000059.4(BRCA2):c.8488-20T>G	rs1593930846
NM_000059.4(BRCA2):c.9257-10dup	rs276174919
NM_007294.4(BRCA1):c.212+17T>C	rs369461674
NM_007294.4(BRCA1):c.81-11T>C	rs767144634

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