List of variants in gene BARD1 reported as uncertain significance for Breast and/or ovarian cancer

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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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.668A>G (p.Glu223Gly)	rs145009419	0.00024
NM_000465.4(BARD1):c.1347A>G (p.Gln449=)	rs373257776	0.00021
NM_000465.4(BARD1):c.127C>A (p.Arg43Ser)	rs752871324	0.00006
NM_000465.4(BARD1):c.1793C>A (p.Thr598Asn)	rs376256852	0.00006
NM_000465.4(BARD1):c.716T>A (p.Leu239Gln)	rs200359745	0.00006
NM_000465.4(BARD1):c.1877A>G (p.Asn626Ser)	rs587781443	0.00004
NM_000465.4(BARD1):c.2252G>A (p.Arg751Gln)	rs587782246	0.00003
NM_000465.4(BARD1):c.568G>A (p.Asp190Asn)	rs369561166	0.00003
NM_000465.4(BARD1):c.159T>C (p.Cys53=)	rs201708813	0.00002
NM_000465.4(BARD1):c.1016G>A (p.Ser339Asn)	rs201261729	0.00001
NM_000465.4(BARD1):c.161C>G (p.Thr54Ser)	rs879253878	0.00001
NM_000465.4(BARD1):c.*8A>G
NM_000465.4(BARD1):c.1568+6T>A	rs1553619192
NM_000465.4(BARD1):c.157T>G (p.Cys53Gly)	rs1354779388
NM_000465.4(BARD1):c.505A>G (p.Ile169Val)	rs765494437
NM_000465.4(BARD1):c.941T>C (p.Leu314Ser)	rs199857391

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