List of variants in gene BARD1 reported as benign by Illumina Laboratory Services, Illumina

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.1518T>C (p.His506=)	rs2070093	0.74904
NM_000465.4(BARD1):c.1134G>C (p.Arg378Ser)	rs2229571	0.53291
NM_000465.4(BARD1):c.1568+14C>T	rs5031011	0.34966
NM_000465.4(BARD1):c.70C>T (p.Pro24Ser)	rs1048108	0.32854
NM_000465.4(BARD1):c.1053G>C (p.Thr351=)	rs2070096	0.19573
NM_000465.4(BARD1):c.1670G>C (p.Cys557Ser)	rs28997576	0.01443
NM_000465.4(BARD1):c.609A>C (p.Gly203=)	rs28997574	0.00787
NM_000465.4(BARD1):c.1738G>A (p.Glu580Lys)	rs35306212	0.00455
NM_000465.4(BARD1):c.722C>G (p.Ser241Cys)	rs3738885	0.00006

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