List of variants in gene combination BRCA1, LOC126862571 reported as likely pathogenic for Breast and/or ovarian cancer

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.3690dup (p.Phe1231fs)	rs1567790559
NM_007294.4(BRCA1):c.3997del (p.Val1333fs)
NM_007294.4(BRCA1):c.4085dup (p.Asp1362fs)	rs2053470202

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