List of variants in gene BARD1 reported as uncertain significance by Cancer Genomics Group, Japanese Foundation For Cancer Research

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.773T>C (p.Ile258Thr)	rs146223579	0.00004
NM_000465.4(BARD1):c.556A>G (p.Ser186Gly)	rs16852741	0.00003
NM_000465.4(BARD1):c.233G>A (p.Cys78Tyr)	rs199780731	0.00001
NM_000465.4(BARD1):c.95G>T (p.Gly32Val)	rs587782675	0.00001
NM_000465.4(BARD1):c.128G>C (p.Arg43Pro)	rs1060501305
NM_000465.4(BARD1):c.1309A>G (p.Ile437Val)	rs764592698
NM_000465.4(BARD1):c.1819GTT[2] (p.Val609del)	rs927014703

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