List of variants in gene BARD1 reported as pathogenic by Sema4, Sema4

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1921C>T (p.Arg641Ter)	rs587781948	0.00004
NM_000465.4(BARD1):c.1690C>T (p.Gln564Ter)	rs587780021	0.00003
NM_000465.4(BARD1):c.1652C>G (p.Ser551Ter)	rs587781707	0.00001
NM_000465.4(BARD1):c.623dup (p.Lys209fs)	rs587780033
NM_000465.4(BARD1):c.624dup (p.Lys209fs)	rs1553622558

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