List of variants in gene combination BRCA1, LOC111589215 reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.-86C>T	rs143160357	0.00077
NM_007294.4(BRCA1):c.-125C>T	rs148196794	0.00029
NM_007294.4(BRCA1):c.-75C>G	rs529629382	0.00006
NM_007294.4(BRCA1):c.-20+13C>T	rs770368390	0.00001
NM_007294.4(BRCA1):c.-109A>T	rs886052977
NM_007294.4(BRCA1):c.-22A>G	rs886052976

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