Variants in gene BARD1 with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 15

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HGVS	dbSNP	gnomAD frequency
NM_000465.4(BARD1):c.1569-13C>G	rs587780018	0.00002
NM_000465.4(BARD1):c.1396-5A>G	rs1559410251
NM_000465.4(BARD1):c.1568+5G>A
NM_000465.4(BARD1):c.1569-7T>G	rs1559395026
NM_000465.4(BARD1):c.1677+5G>A	rs587780019
NM_000465.4(BARD1):c.1904-2A>T	rs864622239
NM_000465.4(BARD1):c.2001+3A>G	rs1553612461
NM_000465.4(BARD1):c.2002-1G>A	rs762601855
NM_000465.4(BARD1):c.2002-2A>C	rs876658260
NM_000465.4(BARD1):c.2002-2A>G	rs876658260
NM_000465.4(BARD1):c.2002-2A>T	rs876658260
NM_000465.4(BARD1):c.211T>A (p.Cys71Ser)	rs1060501308
NM_000465.4(BARD1):c.2148_2149del (p.Ile717fs)	rs786203811
NM_000465.4(BARD1):c.215+5_215+8del	rs876658777
NM_000465.4(BARD1):c.247T>C (p.Cys83Arg)	rs1559437198

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