List of variants in gene BARD1 reported as likely pathogenic by Department of Pathology and Laboratory Medicine, Sinai Health System

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.216-1G>T	rs876658905
NM_000465.4(BARD1):c.2215dup (p.Tyr739fs)	rs2469268815
NM_000465.4(BARD1):c.2300_2301del (p.Val767fs)	rs750413473

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