List of variants in gene BARD1 reported as pathogenic by Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1690C>T (p.Gln564Ter)	rs587780021	0.00003
NM_000465.4(BARD1):c.1569-1G>C	rs1574756672
NM_000465.4(BARD1):c.1622C>A (p.Ser541Ter)	rs777937955
NM_000465.4(BARD1):c.1935_1954dup (p.Glu652fs)	rs587780024

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