List of variants in gene BARD1 reported as not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.659T>C (p.Leu220Ser)	rs138593305	0.00013
NM_000465.4(BARD1):c.1127C>T (p.Ser376Leu)	rs587782333	0.00009
NM_000465.4(BARD1):c.946T>G (p.Leu316Val)	rs587782325	0.00005
NM_000465.4(BARD1):c.1877A>G (p.Asn626Ser)	rs587781443	0.00004
NM_000465.4(BARD1):c.97G>C (p.Ala33Pro)	rs587782465	0.00004
NM_000465.4(BARD1):c.1448A>G (p.His483Arg)	rs587781874	0.00001
NM_000465.4(BARD1):c.1808C>A (p.Thr603Lys)	rs730881421	0.00001
NM_000465.4(BARD1):c.1868G>A (p.Gly623Glu)	rs587782252	0.00001
NM_000465.4(BARD1):c.1990A>G (p.Arg664Gly)	rs1064795138	0.00001
NM_000465.4(BARD1):c.2171C>T (p.Ala724Val)	rs587782662	0.00001
NM_000465.4(BARD1):c.614A>G (p.Lys205Arg)	rs587782437	0.00001
NM_000465.4(BARD1):c.673G>T (p.Glu225Ter)	rs1064793049	0.00001
NM_000465.4(BARD1):c.1887G>A (p.Trp629Ter)	rs878854003
NM_000465.4(BARD1):c.1935_1954dup (p.Glu652fs)	rs587780024
NM_000465.4(BARD1):c.273G>A (p.Trp91Ter)	rs2106135008

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