List of variants in gene BARD1 reported as benign by Ambry Genetics

Minimum submission review status:		Collection method:
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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1518T>C (p.His506=)	rs2070093	0.75581
NM_000465.4(BARD1):c.1134G>C (p.Arg378Ser)	rs2229571	0.53291
NM_000465.4(BARD1):c.70C>T (p.Pro24Ser)	rs1048108	0.33242
NM_000465.4(BARD1):c.1053G>C (p.Thr351=)	rs2070096	0.19714
NM_000465.4(BARD1):c.1933T>C (p.Cys645Arg)	rs2228456	0.01986
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.2212A>G (p.Ile738Val)	rs61754118	0.00745
NM_000465.4(BARD1):c.1972C>T (p.Arg658Cys)	rs3738888	0.00668
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.581G>A (p.Arg194Lys)	rs181748854	0.00004
NM_000465.4(BARD1):c.1053G>A (p.Thr351=)	rs2070096
NM_000465.4(BARD1):c.1075_1095del (p.Leu359_Pro365del)	rs28997575
NM_000465.4(BARD1):c.1519G>A (p.Val507Met)	rs2070094
NM_000465.4(BARD1):c.216-14del	rs56130510

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