List of variants in gene BRIP1 reported as likely benign 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.577G>A (p.Val193Ile)	rs4988346	0.00305
NM_032043.3(BRIP1):c.2097+7G>A	rs4988352	0.00271
NM_032043.3(BRIP1):c.584T>C (p.Leu195Pro)	rs4988347	0.00197
NM_032043.3(BRIP1):c.890A>G (p.Lys297Arg)	rs28997570	0.00113
NM_032043.3(BRIP1):c.380-17T>A	rs200050729	0.00034
NM_032043.3(BRIP1):c.-30-3T>C	rs370728413	0.00014
NM_032043.3(BRIP1):c.3444C>A (p.Asp1148Glu)	rs28997573	0.00011
NM_032043.3(BRIP1):c.924A>G (p.Lys308=)	rs374974885	0.00002
NM_032043.3(BRIP1):c.3681T>C (p.His1227=)	rs370581038	0.00001
NM_032043.3(BRIP1):c.618G>T (p.Ser206=)	rs367614726

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