List of variants in gene BRIP1 reported as benign by Institute for Biomarker Research, Medical Diagnostic Laboratories, L.L.C.

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.584T>C (p.Leu195Pro)	rs4988347	0.00197
NM_032043.3(BRIP1):c.2937A>G (p.Lys979=)	rs75091137	0.00194
NM_032043.3(BRIP1):c.3378A>C (p.Glu1126Asp)	rs145855459	0.00076
NM_032043.3(BRIP1):c.317G>A (p.Arg106His)	rs143615668	0.00048
NM_032043.3(BRIP1):c.2440C>T (p.Arg814Cys)	rs201869624	0.00016
NM_032043.3(BRIP1):c.689C>T (p.Ser230Leu)	rs759031349	0.00006
NM_032043.3(BRIP1):c.2830C>G (p.Gln944Glu)	rs140233356	0.00003
NM_032043.3(BRIP1):c.370A>G (p.Thr124Ala)	rs45617634

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