List of variants in gene combination BRCA1, LOC111589215 reported as uncertain significance by Department of Pathology and Laboratory Medicine, Sinai Health System

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: 4

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HGVS	dbSNP	gnomAD frequency
NC_000017.11:g.43125372C>G	rs1438870433	0.00001
NM_007294.4(BRCA1):c.-44C>T	rs1262271602	0.00001
NC_000017.11:g.43125424_43125428del	rs2154580334
NM_007294.4(BRCA1):c.-42T>G	rs544342552

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