List of variants in gene BRIP1 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.1201del (p.Cys401fs)	rs2145307439
NM_032043.3(BRIP1):c.2947del (p.Ile983fs)	rs774684620
NM_032043.3(BRIP1):c.918+2_918+3del	rs2145410258

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