ClinVar Miner

List of variants in gene combination BRCA1, LOC110485084, LOC111589216 reported as uncertain significance for Hereditary cancer-predisposing syndrome

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.81-4038G>A	rs961274781	0.00009
NM_007294.4(BRCA1):c.80+4041C>T	rs186936074

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