List of variants in gene BRCA1 reported as likely pathogenic for Breast carcinoma

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_007294.4(BRCA1):c.1061del (p.Asn354fs)	rs2154478354
NM_007294.4(BRCA1):c.1119_1120insCTGA (p.Thr374fs)	rs2154475092
NM_007294.4(BRCA1):c.2756del (p.Pro919fs)	rs2154361062
NM_007294.4(BRCA1):c.473_547+288del	rs2154527022
NM_007294.4(BRCA1):c.4986+5G>A	rs397509211

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