List of variants in gene BARD1 reported as uncertain significance by Institute of Human Genetics, University of Leipzig Medical Center

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.1693C>T (p.Arg565Cys)	rs587782279	0.00002
NM_000465.4(BARD1):c.2057A>G (p.His686Arg)	rs864622380	0.00001
NM_000465.4(BARD1):c.2216A>G (p.Tyr739Cys)	rs777013688
NM_000465.4(BARD1):c.895A>G (p.Thr299Ala)	rs1694983227

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