List of variants in gene BARD1 reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1568+111A>C	rs5031005	0.02739
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.609A>C (p.Gly203=)	rs28997574	0.00787
NM_000465.4(BARD1):c.1569-56A>G	rs71579853	0.00762
NM_000465.4(BARD1):c.2212A>G (p.Ile738Val)	rs61754118	0.00745
NM_000465.4(BARD1):c.1678-60T>C	rs4986842	0.00636
NM_000465.4(BARD1):c.1903+145G>A	rs146298985	0.00634
NM_000465.4(BARD1):c.2001+224C>T	rs113815630	0.00372
NM_000465.4(BARD1):c.253G>T (p.Val85Leu)	rs370359540	0.00004
NM_000465.4(BARD1):c.1519G>A (p.Val507Met)	rs2070094
NM_000465.4(BARD1):c.1920A>C (p.Leu640=)	rs780901872

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