ClinVar Miner

List of variants in gene combination BRCA1, LOC111589215 reported as pathogenic

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: 3

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HGVS	dbSNP	gnomAD frequency
NC_000017.11:g.(?_43123997)_(43125483_?)del
NG_005905.2:g.(?_92501)_(92714_93868)del
NM_007294.4(BRCA1):c.-107A>T	rs2154580237

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