List of variants in gene BRIP1 reported as uncertain significance for Familial 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_032043.3(BRIP1):c.2120G>T (p.Arg707Leu)	rs200313471
NM_032043.3(BRIP1):c.428A>G (p.Gln143Arg)	rs1603362656
NM_032043.3(BRIP1):c.93+2dup	rs786202125

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