List of variants in gene BARD1 reported as uncertain significance by National Health Laboratory Service, Universitas Academic Hospital and University of the Free State

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1429G>A (p.Val477Met)	rs1024564785	0.00001
NM_000465.4(BARD1):c.2029T>C (p.Phe677Leu)	rs746790711	0.00001
NM_000465.4(BARD1):c.2251C>T (p.Arg751Trp)	rs139785364	0.00001
NM_000465.4(BARD1):c.1118G>A (p.Gly373Asp)	rs568305044
NM_000465.4(BARD1):c.1153G>A (p.Asp385Asn)	rs587782436
NM_000465.4(BARD1):c.1352G>A (p.Gly451Glu)	rs771410310
NM_000465.4(BARD1):c.1513G>A (p.Gly505Arg)	rs864622240
NM_000465.4(BARD1):c.2191C>G (p.Arg731Gly)	rs76744638
NM_000465.4(BARD1):c.401A>G (p.Asn134Ser)	rs1559426297

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