List of variants in gene combination BRCA1, LOC111589215 reported as uncertain significance for Hereditary breast ovarian cancer syndrome

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.-20+1G>C	rs769633464	0.00001
NC_000017.10:g.(?_41276014)_(41277500_?)dup
NC_000017.10:g.(?_41277288)_(41277500_?)dup
NC_000017.11:g.43125428G>A
NC_000017.11:g.43125428G>C
NM_007294.4(BRCA1):c.-109A>T	rs886052977
NM_007294.4(BRCA1):c.-20+10T>C
NM_007294.4(BRCA1):c.-20+2T>C	rs1567824383
NM_007294.4(BRCA1):c.-20+2dup
NM_007294.4(BRCA1):c.-20+3A>G	rs1064795882
NM_007294.4(BRCA1):c.-20+3A>T	rs1064795882
NM_007294.4(BRCA1):c.-20+6A>G
NM_007294.4(BRCA1):c.-70A>G

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