List of variants in gene BARD1 reported as benign by Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1933T>C (p.Cys645Arg)	rs2228456	0.01986
NM_000465.4(BARD1):c.1314+29C>G	rs71579845	0.01475
NM_000465.4(BARD1):c.1670G>C (p.Cys557Ser)	rs28997576	0.01443
NM_000465.4(BARD1):c.609A>C (p.Gly203=)	rs28997574	0.00787
NM_000465.4(BARD1):c.1738G>A (p.Glu580Lys)	rs35306212	0.00424
NM_000465.4(BARD1):c.722C>G (p.Ser241Cys)	rs3738885	0.00027
NM_000465.4(BARD1):c.1075_1095del (p.Leu359_Pro365del)	rs28997575
NM_000465.4(BARD1):c.216-14del	rs56130510
NM_000465.4(BARD1):c.216-29dup	rs56130510
NM_000465.4(BARD1):c.216-37T>C

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