List of variants in gene BARD1 reported as likely benign for Malignant tumor of breast

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1670G>C (p.Cys557Ser)	rs28997576	0.01443
NM_000465.4(BARD1):c.1972C>T (p.Arg658Cys)	rs3738888	0.00668
NM_000465.4(BARD1):c.1977A>G (p.Arg659=)	rs147215925	0.00230
NM_000465.4(BARD1):c.620A>G (p.Lys207Arg)	rs34969857	0.00212
NM_000465.4(BARD1):c.2282G>A (p.Ser761Asn)	rs142155101	0.00149
NM_000465.4(BARD1):c.1515G>T (p.Gly505=)	rs139721211	0.00028
NM_000465.4(BARD1):c.346C>T (p.His116Tyr)	rs144856889	0.00027
NM_000465.4(BARD1):c.722C>G (p.Ser241Cys)	rs3738885	0.00027
NM_000465.4(BARD1):c.1554C>T (p.Ala518=)	rs139612775	0.00015
NM_000465.4(BARD1):c.1203T>C (p.Ser401=)	rs370553043	0.00013
NM_000465.4(BARD1):c.1568+15G>T	rs145936354	0.00010
NM_000465.4(BARD1):c.2002-11C>T	rs187240320	0.00010
NM_000465.4(BARD1):c.253G>T (p.Val85Leu)	rs370359540	0.00004
NM_000465.4(BARD1):c.365-7C>T	rs745929983	0.00004
NM_000465.4(BARD1):c.2280G>A (p.Ser760=)	rs749959440	0.00003
NM_000465.4(BARD1):c.1497C>T (p.His499=)	rs760665188	0.00001
NM_000465.4(BARD1):c.130C>T (p.Leu44=)	rs876658807
NM_000465.4(BARD1):c.1635A>G (p.Leu545=)	rs786203364

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