ClinVar Miner

List of variants in gene BRIP1 reported as likely benign by Institute of Human Genetics, University of Leipzig Medical Center

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.2097+8A>C	rs730881642	0.00001
NM_032043.3(BRIP1):c.3737C>T (p.Pro1246Leu)	rs876660074

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