List of variants in gene BRIP1 reported as pathogenic by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.1741C>T (p.Arg581Ter)	rs780020495	0.00002
NM_032043.3(BRIP1):c.1236del (p.Val413fs)	rs863224525
NM_032043.3(BRIP1):c.1629-1G>A	rs1060501757
NM_032043.3(BRIP1):c.2990_2993del (p.Thr997fs)	rs771028677

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