List of variants in gene BARD1 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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.668A>G (p.Glu223Gly)	rs145009419	0.00025
NM_000465.4(BARD1):c.2291T>C (p.Ile764Thr)	rs587780030	0.00004
NM_000465.4(BARD1):c.1226C>G (p.Ser409Cys)	rs786202226	0.00001
NM_000465.4(BARD1):c.30_44dup (p.Gln11_Arg15dup)	rs587781297
NM_000465.4(BARD1):c.38G>C (p.Arg13Thr)	rs587781713

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