List of variants in gene BRCA1 reported as likely pathogenic by Genomic Center, National Cancer Institute

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
NM_007294.4(BRCA1):c.1015_1016del (p.Lys339fs)
NM_007294.4(BRCA1):c.2857del (p.Cys953fs)	rs397509019
NM_007294.4(BRCA1):c.4526del (p.Tyr1509fs)	rs2154020080

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