List of variants in gene BRIP1 reported as 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.2244C>G (p.Tyr748Ter)	rs1257401983
NM_032043.3(BRIP1):c.2992_2995del (p.Lys998fs)	rs786203717
NM_032043.3(BRIP1):c.507+1G>T	rs2145761239

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