List of variants in gene combination BRCA1, LOC111589215 reported as benign by Evidence-based Network for the Interpretation of Germline Mutant Alleles (ENIGMA)

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_007294.4(BRCA1):c.-20+101C>G	rs799905	0.51032
NM_007294.4(BRCA1):c.-20+336C>T	rs8176076	0.01526
NM_007294.4(BRCA1):c.-192T>C	rs113323025	0.00510
NM_001408458.1(BRCA1):c.-61-9745G>A	rs112960339	0.00509
NM_007294.4(BRCA1):c.-20+530G>A	rs111462026	0.00507
NM_007294.4(BRCA1):c.-20+185T>G	rs55680227	0.00487
NM_007294.4(BRCA1):c.-20+494CAAAA[5]	rs572878542

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