List of variants in gene BARD1 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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.2183C>T (p.Ser728Phe)	rs13389423	0.00006
NM_000465.4(BARD1):c.1207A>G (p.Ser403Gly)	rs1060501286
NM_000465.4(BARD1):c.1314G>A (p.Lys438=)	rs1559423185
NM_000465.4(BARD1):c.1559G>A (p.Arg520Lys)	rs2469442414

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